Linked Data
ClinVar Variation Id:
373769
dbSNP Id:
rs763147599
ExAC:
19:11227603 G / A
gnomAD v2:
19-11227603-G-A
gnomAD v4:
19-11116927-G-A
ERepo:
CA036598/MONDO:0007750/013
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11116927G>A , CM000681.2:g.11116927G>A | GRCh38 |
| NC_000019.9:g.11227603G>A , CM000681.1:g.11227603G>A | GRCh37 |
| NC_000019.8:g.11088603G>A | NCBI36 |
| NG_009060.1:g.32547G>A , LRG_274:g.32547G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2032G>A | ENSP00000252444.6:p.Gly678Arg | |
| ENST00000559340.2:c.1705+715G>A | ENSP00000453696.2:n.1705+715G>A | |
| ENST00000560467.2:c.1654G>A | ENSP00000453513.2:p.Gly552Arg | |
| ENST00000558518.6:c.1774G>A MANE Select | ENSP00000454071.1:p.Gly592Arg | |
| ENST00000252444.9:c.2028G>A | ||
| ENST00000455727.6:c.1270G>A | ENSP00000397829.2:p.Gly424Arg | |
| ENST00000535915.5:c.1651G>A | ENSP00000440520.1:p.Gly551Arg | |
| ENST00000545707.5:c.1393G>A | ENSP00000437639.1:p.Gly465Arg | |
| ENST00000557933.5:c.1774G>A | ENSP00000453557.1:p.Gly592Arg | |
| ENST00000558013.5:c.1774G>A | ENSP00000453346.1:p.Gly592Arg | |
| ENST00000558518.5:c.1774G>A | ENSP00000454071.1:p.Gly592Arg | |
| ENST00000559340.1:c.426+715G>A | ||
| NM_000527.4:c.1774G>A , LRG_274t1:c.1774G>A | NP_000518.1:p.Gly592Arg | |
| NM_001195798.1:c.1774G>A | NP_001182727.1:p.Gly592Arg | |
| NM_001195799.1:c.1651G>A | NP_001182728.1:p.Gly551Arg | |
| NM_001195800.1:c.1270G>A | NP_001182729.1:p.Gly424Arg | |
| NM_001195803.1:c.1393G>A | NP_001182732.1:p.Gly465Arg | |
| XM_011528010.1:c.1774G>A | XP_011526312.1:p.Gly592Arg | |
| XM_011528011.1:c.1393G>A | XP_011526313.1:p.Gly465Arg | |
| XR_244074.2:n.1855+715G>A | ||
| XM_011528010.2:c.1774G>A | XP_011526312.1:p.Gly592Arg | |
| XR_001753685.2:n.1891G>A | ||
| XR_001753686.2:n.1822+715G>A | ||
| NM_000527.5:c.1774G>A MANE Select | NP_000518.1:p.Gly592Arg | |
| NM_001195798.2:c.1774G>A | NP_001182727.1:p.Gly592Arg | |
| NM_001195799.2:c.1651G>A | NP_001182728.1:p.Gly551Arg | |
| NM_001195800.2:c.1270G>A | NP_001182729.1:p.Gly424Arg | |
| NM_001195803.2:c.1393G>A | NP_001182732.1:p.Gly465Arg |