Linked Data
ClinVar Variation Id:
381663
dbSNP Id:
rs145798311
ExAC:
16:88909177 G / A
gnomAD v2:
16-88909177-G-A
gnomAD v3:
16-88842769-G-A
gnomAD v4:
16-88842769-G-A
COSMIC:
COSM33117
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88842769G>A , CM000678.2:g.88842769G>A | GRCh38 |
| NC_000016.9:g.88909177G>A , CM000678.1:g.88909177G>A | GRCh37 |
| NC_000016.8:g.87436678G>A | NCBI36 |
| NG_008667.1:g.19198C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268695.10:c.181C>T MANE Select | ENSP00000268695.5:p.Arg61Trp | |
| ENST00000268695.9:c.181C>T | ENSP00000268695.5:p.Arg61Trp | |
| ENST00000562593.5:n.2856C>T | ||
| ENST00000562831.1:c.29-798C>T | ENSP00000455174.1:n.29-798C>T | |
| ENST00000565364.1:n.316C>T | ||
| ENST00000567525.5:c.70-798C>T | ENSP00000454484.1:n.70-798C>T | |
| ENST00000568613.5:c.300C>T | ENSP00000457921.1:n.300C>T | |
| NM_000512.4:c.181C>T | NP_000503.1:p.Arg61Trp | |
| XM_005256301.2:c.181C>T | XP_005256358.1:p.Arg61Trp | |
| XM_005256302.1:c.199C>T | XP_005256359.1:p.Arg67Trp | |
| XM_011522982.1:c.199C>T | XP_011521284.1:p.Arg67Trp | |
| XM_011522984.1:c.199C>T | XP_011521286.1:p.Arg67Trp | |
| NM_001323543.1:c.-311-798C>T | NP_001310472.1:n.-311-798C>T | |
| NM_001323544.1:c.199C>T | NP_001310473.1:p.Arg67Trp | |
| XM_005256301.3:c.181C>T | XP_005256358.1:p.Arg61Trp | |
| XM_011522982.2:c.199C>T | XP_011521284.1:p.Arg67Trp | |
| XM_017023111.2:c.199C>T | XP_016878600.1:p.Arg67Trp | |
| XM_017023112.2:c.199C>T | XP_016878601.1:p.Arg67Trp | |
| XM_017023113.1:c.-311-798C>T | XP_016878602.1:n.-311-798C>T | |
| NM_000512.5:c.181C>T MANE Select | NP_000503.1:p.Arg61Trp | |
| NM_001323543.2:c.-311-798C>T | NP_001310472.1:n.-311-798C>T | |
| NM_001323544.2:c.199C>T | NP_001310473.1:p.Arg67Trp |