Linked Data
ClinVar Variation Id:
971637
dbSNP Id:
rs370733771
ExAC:
9:37429746 C / T
gnomAD v2:
9-37429746-C-T
gnomAD v3:
9-37429749-C-T
gnomAD v4:
9-37429749-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37429749C>T , CM000671.2:g.37429749C>T | GRCh38 |
| NC_000009.11:g.37429746C>T , CM000671.1:g.37429746C>T | GRCh37 |
| NC_000009.10:g.37419746C>T | NCBI36 |
| NG_008135.1:g.12040C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318158.11:c.511C>T MANE Select | ENSP00000313432.6:p.Arg171Cys | |
| ENST00000318158.10:c.511C>T | ENSP00000313432.6:p.Arg171Cys | |
| ENST00000377824.8:n.548C>T | ||
| ENST00000460882.5:n.538C>T | ||
| ENST00000480596.5:n.1212C>T | ||
| ENST00000491488.5:n.216C>T | ||
| ENST00000494290.1:c.82C>T | ENSP00000432021.1:p.Arg28Cys | |
| ENST00000497693.1:n.2044C>T | ||
| ENST00000607784.1:c.511C>T | ENSP00000475569.1:p.Arg171Cys | |
| NM_012203.1:c.511C>T | NP_036335.1:p.Arg171Cys | |
| XM_005251631.1:c.190C>T | XP_005251688.1:p.Arg64Cys | |
| XM_011518073.1:c.109C>T | XP_011516375.1:p.Arg37Cys | |
| XR_929374.1:n.956C>T | ||
| XM_017015320.2:c.511C>T | XP_016870809.1:p.Arg171Cys | |
| XM_017015321.2:c.511C>T | XP_016870810.1:p.Arg171Cys | |
| XM_017015323.2:c.109C>T | XP_016870812.1:p.Arg37Cys | |
| XM_024447716.1:c.784C>T | XP_024303484.1:p.Arg262Cys | |
| XM_024447717.1:c.784C>T | XP_024303485.1:p.Arg262Cys | |
| XR_002956828.1:n.799C>T | ||
| XR_002956829.1:n.799C>T | ||
| XR_002956830.1:n.570C>T | ||
| XR_002956831.1:n.245C>T | ||
| XR_002956832.1:n.930C>T | ||
| NM_012203.2:c.511C>T MANE Select | NP_036335.1:p.Arg171Cys |