Linked Data
ClinVar Variation Id:
2498755
ClinVar RCV Id:
RCV003222964
dbSNP Id:
rs2077283735
gnomAD v3:
19-11105604-T-G
gnomAD v4:
19-11105604-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11105604T>G , CM000681.2:g.11105604T>G | GRCh38 |
| NC_000019.9:g.11216280T>G , CM000681.1:g.11216280T>G | GRCh37 |
| NC_000019.8:g.11077280T>G | NCBI36 |
| NG_009060.1:g.21224T>G , LRG_274:g.21224T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.952+4T>G | ENSP00000252444.6:n.952+4T>G | |
| ENST00000559340.2:c.694+4T>G | ENSP00000453696.2:n.694+4T>G | |
| ENST00000560467.2:c.694+4T>G | ENSP00000453513.2:n.694+4T>G | |
| ENST00000558518.6:c.694+4T>G MANE Select | ENSP00000454071.1:n.694+4T>G | |
| ENST00000252444.9:c.948+4T>G | ||
| ENST00000455727.6:c.314-1788T>G | ENSP00000397829.2:n.314-1788T>G | |
| ENST00000535915.5:c.571+4T>G | ENSP00000440520.1:n.571+4T>G | |
| ENST00000545707.5:c.314-961T>G | ENSP00000437639.1:n.314-961T>G | |
| ENST00000557933.5:c.694+4T>G | ENSP00000453557.1:n.694+4T>G | |
| ENST00000558013.5:c.694+4T>G | ENSP00000453346.1:n.694+4T>G | |
| ENST00000558518.5:c.694+4T>G | ENSP00000454071.1:n.694+4T>G | |
| ENST00000560467.1:c.294+4T>G | ||
| NM_000527.4:c.694+4T>G , LRG_274t1:c.694+4T>G | NP_000518.1:n.694+4T>G | |
| NM_001195798.1:c.694+4T>G | NP_001182727.1:n.694+4T>G | |
| NM_001195799.1:c.571+4T>G | NP_001182728.1:n.571+4T>G | |
| NM_001195800.1:c.314-1788T>G | NP_001182729.1:n.314-1788T>G | |
| NM_001195803.1:c.314-961T>G | NP_001182732.1:n.314-961T>G | |
| XM_011528010.1:c.694+4T>G | XP_011526312.1:n.694+4T>G | |
| XM_011528011.1:c.314-961T>G | XP_011526313.1:n.314-961T>G | |
| XR_244074.2:n.844+4T>G | ||
| XM_011528010.2:c.694+4T>G | XP_011526312.1:n.694+4T>G | |
| XR_001753685.2:n.811+4T>G | ||
| XR_001753686.2:n.811+4T>G | ||
| NM_000527.5:c.694+4T>G MANE Select | NP_000518.1:n.694+4T>G | |
| NM_001195798.2:c.694+4T>G | NP_001182727.1:n.694+4T>G | |
| NM_001195799.2:c.571+4T>G | NP_001182728.1:n.571+4T>G | |
| NM_001195800.2:c.314-1788T>G | NP_001182729.1:n.314-1788T>G | |
| NM_001195803.2:c.314-961T>G | NP_001182732.1:n.314-961T>G |