Linked Data
ClinVar Variation Id:
280960
dbSNP Id:
rs886042058
gnomAD v3:
16-88836265-T-C
gnomAD v4:
16-88836265-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88836265T>C , CM000678.2:g.88836265T>C | GRCh38 |
| NC_000016.9:g.88902673T>C , CM000678.1:g.88902673T>C | GRCh37 |
| NC_000016.8:g.87430174T>C | NCBI36 |
| NG_008667.1:g.25702A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268695.10:c.569A>G MANE Select | ENSP00000268695.5:p.Tyr190Cys | |
| ENST00000268695.9:c.569A>G | ENSP00000268695.5:p.Tyr190Cys | |
| ENST00000561812.1:n.525A>G | ||
| ENST00000562593.5:n.3978A>G | ||
| ENST00000562831.1:c.353A>G | ENSP00000455174.1:p.Tyr118Cys | |
| ENST00000562931.5:n.157A>G | ||
| ENST00000566563.1:n.271A>G | ||
| ENST00000567525.5:c.250A>G | ENSP00000454484.1:n.250A>G | |
| ENST00000568613.5:c.688A>G | ENSP00000457921.1:n.688A>G | |
| NM_000512.4:c.569A>G | NP_000503.1:p.Tyr190Cys | |
| XM_005256301.2:c.569A>G | XP_005256358.1:p.Tyr190Cys | |
| XM_005256302.1:c.587A>G | XP_005256359.1:p.Tyr196Cys | |
| XM_011522982.1:c.587A>G | XP_011521284.1:p.Tyr196Cys | |
| XM_011522984.1:c.587A>G | XP_011521286.1:p.Tyr196Cys | |
| NM_001323543.1:c.14A>G | NP_001310472.1:p.Tyr5Cys | |
| NM_001323544.1:c.587A>G | NP_001310473.1:p.Tyr196Cys | |
| XM_005256301.3:c.569A>G | XP_005256358.1:p.Tyr190Cys | |
| XM_011522982.2:c.587A>G | XP_011521284.1:p.Tyr196Cys | |
| XM_017023111.2:c.587A>G | XP_016878600.1:p.Tyr196Cys | |
| XM_017023112.2:c.587A>G | XP_016878601.1:p.Tyr196Cys | |
| XM_017023113.1:c.14A>G | XP_016878602.1:p.Tyr5Cys | |
| NM_000512.5:c.569A>G MANE Select | NP_000503.1:p.Tyr190Cys | |
| NM_001323543.2:c.14A>G | NP_001310472.1:p.Tyr5Cys | |
| NM_001323544.2:c.587A>G | NP_001310473.1:p.Tyr196Cys |