Linked Data
ClinVar Variation Id:
14735
ClinVar RCV Id:
RCV000015856
dbSNP Id:
rs121912463
ExAC:
17:73732158 T / C
gnomAD v2:
17-73732158-T-C
gnomAD v4:
17-75736077-T-C
PubMed:
PMID:9792864
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.75736077T>C , CM000679.2:g.75736077T>C | GRCh38 |
| NC_000017.10:g.73732158T>C , CM000679.1:g.73732158T>C | GRCh37 |
| NC_000017.9:g.71243753T>C | NCBI36 |
| NG_007372.1:g.19643T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000449880.7:c.1684T>C | ENSP00000400217.2:p.Cys562Arg | |
| ENST00000200181.8:c.1684T>C MANE Select | ENSP00000200181.3:p.Cys562Arg | |
| ENST00000200181.7:c.1684T>C | ENSP00000200181.3:p.Cys562Arg | |
| ENST00000449880.6:c.1684T>C | ENSP00000400217.2:p.Cys562Arg | |
| ENST00000450894.7:c.1684T>C | ENSP00000405536.3:p.Cys562Arg | |
| ENST00000579662.5:c.1684T>C | ENSP00000463651.1:p.Cys562Arg | |
| ENST00000580542.5:n.1749T>C | ||
| ENST00000582629.1:c.265+6700T>C | ENSP00000463788.1:n.265+6700T>C | |
| ENST00000584374.1:n.461T>C | ||
| ENST00000584558.5:n.1684T>C | ||
| NM_000213.3:c.1684T>C | NP_000204.3:p.Cys562Arg | |
| NM_001005619.1:c.1684T>C | NP_001005619.1:p.Cys562Arg | |
| NM_001005731.1:c.1684T>C | NP_001005731.1:p.Cys562Arg | |
| XM_005257309.2:c.1684T>C | XP_005257366.1:p.Cys562Arg | |
| XM_005257311.3:c.1684T>C | XP_005257368.1:p.Cys562Arg | |
| XM_005257312.2:c.1684T>C | XP_005257369.1:p.Cys562Arg | |
| XM_006721866.2:c.1789T>C | XP_006721929.1:p.Cys597Arg | |
| XM_006721867.2:c.1789T>C | XP_006721930.1:p.Cys597Arg | |
| XM_006721868.2:c.1789T>C | XP_006721931.1:p.Cys597Arg | |
| XM_006721870.2:c.1789T>C | XP_006721933.1:p.Cys597Arg | |
| XM_011524751.1:c.1789T>C | XP_011523053.1:p.Cys597Arg | |
| NM_000213.4:c.1684T>C | NP_000204.3:p.Cys562Arg | |
| NM_001005731.2:c.1684T>C | NP_001005731.1:p.Cys562Arg | |
| NM_001321123.1:c.1684T>C | NP_001308052.1:p.Cys562Arg | |
| XM_005257311.4:c.1684T>C | XP_005257368.1:p.Cys562Arg | |
| XM_006721866.3:c.1789T>C | XP_006721929.1:p.Cys597Arg | |
| XM_006721867.3:c.1789T>C | XP_006721930.1:p.Cys597Arg | |
| XM_006721868.3:c.1789T>C | XP_006721931.1:p.Cys597Arg | |
| XM_006721870.3:c.1789T>C | XP_006721933.1:p.Cys597Arg | |
| XM_011524751.2:c.1789T>C | XP_011523053.1:p.Cys597Arg | |
| NM_000213.5:c.1684T>C MANE Select | NP_000204.3:p.Cys562Arg | |
| NM_001005731.3:c.1684T>C | NP_001005731.1:p.Cys562Arg | |
| NM_001321123.2:c.1684T>C | NP_001308052.1:p.Cys562Arg |