Linked Data
ClinVar Variation Id:
252308
dbSNP Id:
rs879255192
ExAC:
19:11238775 G / A
gnomAD v2:
19-11238775-G-A
gnomAD v3:
19-11128099-G-A
gnomAD v4:
19-11128099-G-A
MyVariant Identifiers:
chr19:g.11238775G>A (hg19)
chr19:g.11238775_11238785delinsAGTCCCCCAGC (hg19)
chr19:g.11128099G>A (hg38)
ERepo:
CA9204959/MONDO:0007750/013
PubMed:
PMID:20809525
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11128099G>A , CM000681.2:g.11128099G>A | GRCh38 |
| NC_000019.9:g.11238775G>A , CM000681.1:g.11238775G>A | GRCh37 |
| NC_000019.8:g.11099775G>A | NCBI36 |
| NG_009060.1:g.43719G>A , LRG_274:g.43719G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2647+14G>A | ENSP00000252444.6:n.2647+14G>A | |
| ENST00000559340.2:c.*458+14G>A | ENSP00000453696.2:n.*458+14G>A | |
| ENST00000560467.2:c.2269+14G>A | ENSP00000453513.2:n.2269+14G>A | |
| ENST00000558518.6:c.2389+14G>A MANE Select | ENSP00000454071.1:n.2389+14G>A | |
| ENST00000252444.9:c.2643+14G>A | ||
| ENST00000455727.6:c.1885+14G>A | ENSP00000397829.2:n.1885+14G>A | |
| ENST00000535915.5:c.2266+14G>A | ENSP00000440520.1:n.2266+14G>A | |
| ENST00000545707.5:c.1855+14G>A | ENSP00000437639.1:n.1855+14G>A | |
| ENST00000557933.5:c.2389+14G>A | ENSP00000453557.1:n.2389+14G>A | |
| ENST00000558013.5:c.2389+14G>A | ENSP00000453346.1:n.2389+14G>A | |
| ENST00000558518.5:c.2389+14G>A | ENSP00000454071.1:n.2389+14G>A | |
| ENST00000560628.1:n.108+445G>A | ||
| NM_000527.4:c.2389+14G>A , LRG_274t1:c.2389+14G>A | NP_000518.1:n.2389+14G>A | |
| NM_001195798.1:c.2389+14G>A | NP_001182727.1:n.2389+14G>A | |
| NM_001195799.1:c.2266+14G>A | NP_001182728.1:n.2266+14G>A | |
| NM_001195800.1:c.1885+14G>A | NP_001182729.1:n.1885+14G>A | |
| NM_001195803.1:c.1855+14G>A | NP_001182732.1:n.1855+14G>A | |
| XM_011528010.1:c.2312-1414G>A | XP_011526312.1:n.2312-1414G>A | |
| XM_011528011.1:c.2008+14G>A | XP_011526313.1:n.2008+14G>A | |
| XR_244074.2:n.2399+14G>A | ||
| XM_011528010.2:c.2312-1414G>A | XP_011526312.1:n.2312-1414G>A | |
| XR_001753685.2:n.2723+14G>A | ||
| XR_001753686.2:n.2366+14G>A | ||
| NM_000527.5:c.2389+14G>A MANE Select | NP_000518.1:n.2389+14G>A | |
| NM_001195798.2:c.2389+14G>A | NP_001182727.1:n.2389+14G>A | |
| NM_001195799.2:c.2266+14G>A | NP_001182728.1:n.2266+14G>A | |
| NM_001195800.2:c.1885+14G>A | NP_001182729.1:n.1885+14G>A | |
| NM_001195803.2:c.1855+14G>A | NP_001182732.1:n.1855+14G>A |