Linked Data
ClinVar Variation Id:
1101469
ClinVar RCV Id:
RCV001424441
dbSNP Id:
rs2077414954
MyVariant Identifiers:
chr19:g.11224229C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11113553C>G , CM000681.2:g.11113553C>G | GRCh38 |
| NC_000019.9:g.11224229C>G , CM000681.1:g.11224229C>G | GRCh37 |
| NC_000019.8:g.11085229C>G | NCBI36 |
| NG_009060.1:g.29173C>G , LRG_274:g.29173C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1635C>G | ENSP00000252444.6:p.Ala545= | |
| ENST00000559340.2:c.1377C>G | ENSP00000453696.2:p.Ala459= | |
| ENST00000560467.2:c.1257C>G | ENSP00000453513.2:p.Ala419= | |
| ENST00000558518.6:c.1377C>G MANE Select | ENSP00000454071.1:p.Ala459= | |
| ENST00000252444.9:c.1631C>G | ||
| ENST00000455727.6:c.873C>G | ENSP00000397829.2:p.Ala291= | |
| ENST00000535915.5:c.1254C>G | ENSP00000440520.1:p.Ala418= | |
| ENST00000545707.5:c.996C>G | ENSP00000437639.1:p.Ala332= | |
| ENST00000557933.5:c.1377C>G | ENSP00000453557.1:p.Ala459= | |
| ENST00000558013.5:c.1377C>G | ENSP00000453346.1:p.Ala459= | |
| ENST00000558518.5:c.1377C>G | ENSP00000454071.1:p.Ala459= | |
| ENST00000559340.1:c.98C>G | ||
| ENST00000560467.1:c.857C>G | ||
| NM_000527.4:c.1377C>G , LRG_274t1:c.1377C>G | NP_000518.1:p.Ala459= | |
| NM_001195798.1:c.1377C>G | NP_001182727.1:p.Ala459= | |
| NM_001195799.1:c.1254C>G | NP_001182728.1:p.Ala418= | |
| NM_001195800.1:c.873C>G | NP_001182729.1:p.Ala291= | |
| NM_001195803.1:c.996C>G | NP_001182732.1:p.Ala332= | |
| XM_011528010.1:c.1377C>G | XP_011526312.1:p.Ala459= | |
| XM_011528011.1:c.996C>G | XP_011526313.1:p.Ala332= | |
| XR_244074.2:n.1527C>G | ||
| XM_011528010.2:c.1377C>G | XP_011526312.1:p.Ala459= | |
| XR_001753685.2:n.1494C>G | ||
| XR_001753686.2:n.1494C>G | ||
| NM_000527.5:c.1377C>G MANE Select | NP_000518.1:p.Ala459= | |
| NM_001195798.2:c.1377C>G | NP_001182727.1:p.Ala459= | |
| NM_001195799.2:c.1254C>G | NP_001182728.1:p.Ala418= | |
| NM_001195800.2:c.873C>G | NP_001182729.1:p.Ala291= | |
| NM_001195803.2:c.996C>G | NP_001182732.1:p.Ala332= |