Linked Data
ClinVar Variation Id:
1663052
ClinVar RCV Id:
RCV002179298
dbSNP Id:
rs2077411000
gnomAD v3:
19-11113405-C-T
gnomAD v4:
19-11113405-C-T
MyVariant Identifiers:
chr19:g.11224081C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11113405C>T , CM000681.2:g.11113405C>T | GRCh38 |
| NC_000019.9:g.11224081C>T , CM000681.1:g.11224081C>T | GRCh37 |
| NC_000019.8:g.11085081C>T | NCBI36 |
| NG_009060.1:g.29025C>T , LRG_274:g.29025C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252444.10:c.1572C>T | ENSP00000252444.6:p.Ser524= | |
| ENST00000559340.2:c.1314C>T | ENSP00000453696.2:p.Ser438= | |
| ENST00000560467.2:c.1194C>T | ENSP00000453513.2:p.Ser398= | |
| ENST00000558518.6:c.1314C>T MANE Select | ENSP00000454071.1:p.Ser438= | |
| ENST00000252444.9:c.1568C>T | ||
| ENST00000455727.6:c.810C>T | ENSP00000397829.2:p.Ser270= | |
| ENST00000535915.5:c.1191C>T | ENSP00000440520.1:p.Ser397= | |
| ENST00000545707.5:c.933C>T | ENSP00000437639.1:p.Ser311= | |
| ENST00000557933.5:c.1314C>T | ENSP00000453557.1:p.Ser438= | |
| ENST00000558013.5:c.1314C>T | ENSP00000453346.1:p.Ser438= | |
| ENST00000558518.5:c.1314C>T | ENSP00000454071.1:p.Ser438= | |
| ENST00000559340.1:c.35C>T | ||
| ENST00000560173.1:n.313C>T | ||
| ENST00000560467.1:c.794C>T | ||
| NM_000527.4:c.1314C>T , LRG_274t1:c.1314C>T | NP_000518.1:p.Ser438= | |
| NM_001195798.1:c.1314C>T | NP_001182727.1:p.Ser438= | |
| NM_001195799.1:c.1191C>T | NP_001182728.1:p.Ser397= | |
| NM_001195800.1:c.810C>T | NP_001182729.1:p.Ser270= | |
| NM_001195803.1:c.933C>T | NP_001182732.1:p.Ser311= | |
| XM_011528010.1:c.1314C>T | XP_011526312.1:p.Ser438= | |
| XM_011528011.1:c.933C>T | XP_011526313.1:p.Ser311= | |
| XR_244074.2:n.1464C>T | ||
| XM_011528010.2:c.1314C>T | XP_011526312.1:p.Ser438= | |
| XR_001753685.2:n.1431C>T | ||
| XR_001753686.2:n.1431C>T | ||
| NM_000527.5:c.1314C>T MANE Select | NP_000518.1:p.Ser438= | |
| NM_001195798.2:c.1314C>T | NP_001182727.1:p.Ser438= | |
| NM_001195799.2:c.1191C>T | NP_001182728.1:p.Ser397= | |
| NM_001195800.2:c.810C>T | NP_001182729.1:p.Ser270= | |
| NM_001195803.2:c.933C>T | NP_001182732.1:p.Ser311= |