Linked Data
ClinVar Variation Id:
492898
ClinVar RCV Id:
RCV000581450
dbSNP Id:
rs201175894
ExAC:
2:31805700 A / C
gnomAD v2:
2-31805700-A-C
gnomAD v3:
2-31580630-A-C
gnomAD v4:
2-31580630-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31580630A>C , CM000664.2:g.31580630A>C | GRCh38 |
| NC_000002.11:g.31805700A>C , CM000664.1:g.31805700A>C | GRCh37 |
| NC_000002.10:g.31659204A>C | NCBI36 |
| NG_008365.1:g.5342T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.271T>G MANE Select | ENSP00000477587.1:p.Tyr91Asp | |
| ENST00000622030.1:c.271T>G | ENSP00000477587.1:p.Tyr91Asp | |
| NM_000348.3:c.271T>G | NP_000339.2:p.Tyr91Asp | |
| XM_011533068.1:c.271T>G | XP_011531370.1:p.Tyr91Asp | |
| XM_011533070.1:c.27-46864T>G | XP_011531372.1:n.27-46864T>G | |
| XM_011533071.1:c.27-46864T>G | XP_011531373.1:n.27-46864T>G | |
| XM_011533072.1:c.27-46864T>G | XP_011531374.1:n.27-46864T>G | |
| XM_011533072.2:c.27-46864T>G | XP_011531374.1:n.27-46864T>G | |
| NM_000348.4:c.271T>G MANE Select | NP_000339.2:p.Tyr91Asp |