Linked Data
ClinVar Variation Id:
2911694
ClinVar RCV Id:
RCV003598696
dbSNP Id:
rs1912005429
gnomAD v4:
16-88835325-A-G
MyVariant Identifiers:
chr16:g.88901733A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88835325A>G , CM000678.2:g.88835325A>G | GRCh38 |
| NC_000016.9:g.88901733A>G , CM000678.1:g.88901733A>G | GRCh37 |
| NC_000016.8:g.87429234A>G | NCBI36 |
| NG_008667.1:g.26642T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268695.10:c.786T>C MANE Select | ENSP00000268695.5:p.Asp262= | |
| ENST00000268695.9:c.786T>C | ENSP00000268695.5:p.Asp262= | |
| ENST00000562593.5:n.4195T>C | ||
| ENST00000562931.5:n.374T>C | ||
| ENST00000567525.5:c.467T>C | ENSP00000454484.1:n.467T>C | |
| ENST00000568613.5:c.905T>C | ENSP00000457921.1:n.905T>C | |
| NM_000512.4:c.786T>C | NP_000503.1:p.Asp262= | |
| XM_005256301.2:c.786T>C | XP_005256358.1:p.Asp262= | |
| XM_005256302.1:c.804T>C | XP_005256359.1:p.Asp268= | |
| XM_011522982.1:c.804T>C | XP_011521284.1:p.Asp268= | |
| XM_011522984.1:c.804T>C | XP_011521286.1:p.Asp268= | |
| NM_001323543.1:c.231T>C | NP_001310472.1:p.Asp77= | |
| NM_001323544.1:c.804T>C | NP_001310473.1:p.Asp268= | |
| XM_005256301.3:c.786T>C | XP_005256358.1:p.Asp262= | |
| XM_011522982.2:c.804T>C | XP_011521284.1:p.Asp268= | |
| XM_017023111.2:c.804T>C | XP_016878600.1:p.Asp268= | |
| XM_017023112.2:c.804T>C | XP_016878601.1:p.Asp268= | |
| XM_017023113.1:c.231T>C | XP_016878602.1:p.Asp77= | |
| NM_000512.5:c.786T>C MANE Select | NP_000503.1:p.Asp262= | |
| NM_001323543.2:c.231T>C | NP_001310472.1:p.Asp77= | |
| NM_001323544.2:c.804T>C | NP_001310473.1:p.Asp268= |