Linked Data
dbSNP Id:
rs960305950
gnomAD v2:
19-11227788-C-A
gnomAD v3:
19-11117112-C-A
gnomAD v4:
19-11117112-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11117112C>A , CM000681.2:g.11117112C>A | GRCh38 |
| NC_000019.9:g.11227788C>A , CM000681.1:g.11227788C>A | GRCh37 |
| NC_000019.8:g.11088788C>A | NCBI36 |
| NG_009060.1:g.32732C>A , LRG_274:g.32732C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2103+114C>A | ENSP00000252444.6:n.2103+114C>A | |
| ENST00000559340.2:c.1705+900C>A | ENSP00000453696.2:n.1705+900C>A | |
| ENST00000560467.2:c.1725+114C>A | ENSP00000453513.2:n.1725+114C>A | |
| ENST00000558518.6:c.1845+114C>A MANE Select | ENSP00000454071.1:n.1845+114C>A | |
| ENST00000252444.9:c.2099+114C>A | ||
| ENST00000455727.6:c.1341+114C>A | ENSP00000397829.2:n.1341+114C>A | |
| ENST00000535915.5:c.1722+114C>A | ENSP00000440520.1:n.1722+114C>A | |
| ENST00000545707.5:c.1464+114C>A | ENSP00000437639.1:n.1464+114C>A | |
| ENST00000557933.5:c.1845+114C>A | ENSP00000453557.1:n.1845+114C>A | |
| ENST00000558013.5:c.1845+114C>A | ENSP00000453346.1:n.1845+114C>A | |
| ENST00000558518.5:c.1845+114C>A | ENSP00000454071.1:n.1845+114C>A | |
| ENST00000559340.1:c.426+900C>A | ||
| NM_000527.4:c.1845+114C>A , LRG_274t1:c.1845+114C>A | NP_000518.1:n.1845+114C>A | |
| NM_001195798.1:c.1845+114C>A | NP_001182727.1:n.1845+114C>A | |
| NM_001195799.1:c.1722+114C>A | NP_001182728.1:n.1722+114C>A | |
| NM_001195800.1:c.1341+114C>A | NP_001182729.1:n.1341+114C>A | |
| NM_001195803.1:c.1464+114C>A | NP_001182732.1:n.1464+114C>A | |
| XM_011528010.1:c.1845+114C>A | XP_011526312.1:n.1845+114C>A | |
| XM_011528011.1:c.1464+114C>A | XP_011526313.1:n.1464+114C>A | |
| XR_244074.2:n.1855+900C>A | ||
| XM_011528010.2:c.1845+114C>A | XP_011526312.1:n.1845+114C>A | |
| XR_001753685.2:n.1962+114C>A | ||
| XR_001753686.2:n.1822+900C>A | ||
| NM_000527.5:c.1845+114C>A MANE Select | NP_000518.1:n.1845+114C>A | |
| NM_001195798.2:c.1845+114C>A | NP_001182727.1:n.1845+114C>A | |
| NM_001195799.2:c.1722+114C>A | NP_001182728.1:n.1722+114C>A | |
| NM_001195800.2:c.1341+114C>A | NP_001182729.1:n.1341+114C>A | |
| NM_001195803.2:c.1464+114C>A | NP_001182732.1:n.1464+114C>A |