Linked Data
ClinVar Variation Id:
366854
dbSNP Id:
rs148778319
ExAC:
9:37426583 C / T
gnomAD v2:
9-37426583-C-T
gnomAD v3:
9-37426586-C-T
gnomAD v4:
9-37426586-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37426586C>T , CM000671.2:g.37426586C>T | GRCh38 |
| NC_000009.11:g.37426583C>T , CM000671.1:g.37426583C>T | GRCh37 |
| NC_000009.10:g.37416583C>T | NCBI36 |
| NG_008135.1:g.8877C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318158.11:c.336C>T MANE Select | ENSP00000313432.6:p.Ala112= | |
| ENST00000318158.10:c.336C>T | ENSP00000313432.6:p.Ala112= | |
| ENST00000377824.8:n.373C>T | ||
| ENST00000460882.5:n.363C>T | ||
| ENST00000487399.5:n.888C>T | ||
| ENST00000491488.5:n.110-1898C>T | ||
| ENST00000493368.5:n.393C>T | ||
| ENST00000607784.1:c.336C>T | ENSP00000475569.1:p.Ala112= | |
| NM_012203.1:c.336C>T | NP_036335.1:p.Ala112= | |
| XM_005251631.1:c.84-1898C>T | XP_005251688.1:n.84-1898C>T | |
| XM_011518073.1:c.-427C>T | XP_011516375.1:n.-427C>T | |
| XR_929374.1:n.421C>T | ||
| XM_017015320.2:c.336C>T | XP_016870809.1:p.Ala112= | |
| XM_017015321.2:c.336C>T | XP_016870810.1:p.Ala112= | |
| XM_017015323.2:c.-427C>T | XP_016870812.1:n.-427C>T | |
| XM_024447716.1:c.609C>T | XP_024303484.1:p.Ala203= | |
| XM_024447717.1:c.609C>T | XP_024303485.1:p.Ala203= | |
| XR_002956828.1:n.624C>T | ||
| XR_002956829.1:n.624C>T | ||
| XR_002956830.1:n.395C>T | ||
| XR_002956831.1:n.139-1898C>T | ||
| XR_002956832.1:n.395C>T | ||
| NM_012203.2:c.336C>T MANE Select | NP_036335.1:p.Ala112= |