Linked Data
ClinVar Variation Id:
373137
dbSNP Id:
rs555794809
ExAC:
7:42187879 G / A
gnomAD v2:
7-42187879-G-A
gnomAD v3:
7-42148280-G-A
gnomAD v4:
7-42148280-G-A
COSMIC:
COSM1622865
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.42148280G>A , CM000669.2:g.42148280G>A | GRCh38 |
| NC_000007.13:g.42187879G>A , CM000669.1:g.42187879G>A | GRCh37 |
| NC_000007.12:g.42154404G>A | NCBI36 |
| NG_008434.1:g.93740C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.313C>T MANE Select | ENSP00000379258.3:p.Arg105Cys | |
| ENST00000642432.1:c.136C>T | ENSP00000495498.1:p.Arg46Cys | |
| ENST00000643264.1:c.136C>T | ENSP00000495207.1:p.Arg46Cys | |
| ENST00000647255.1:c.136C>T | ENSP00000495745.1:p.Arg46Cys | |
| ENST00000677288.1:c.136C>T | ENSP00000503986.1:p.Arg46Cys | |
| ENST00000677605.1:c.313C>T | ENSP00000503743.1:p.Arg105Cys | |
| ENST00000678429.1:c.313C>T | ENSP00000502957.1:p.Arg105Cys | |
| ENST00000395925.7:c.313C>T | ENSP00000379258.3:p.Arg105Cys | |
| ENST00000448703.5:c.313C>T | ENSP00000406135.1:p.Arg105Cys | |
| ENST00000479210.1:n.290C>T | ||
| NM_000168.5:c.313C>T | NP_000159.3:p.Arg105Cys | |
| XM_005249703.1:c.313C>T | XP_005249760.1:p.Arg105Cys | |
| XM_005249704.2:c.313C>T | XP_005249761.1:p.Arg105Cys | |
| XM_011515272.1:c.313C>T | XP_011513574.1:p.Arg105Cys | |
| XM_011515273.1:c.313C>T | XP_011513575.1:p.Arg105Cys | |
| XM_011515274.1:c.136C>T | XP_011513576.1:p.Arg46Cys | |
| XM_011515274.2:c.136C>T | XP_011513576.1:p.Arg46Cys | |
| XM_017011997.1:c.310C>T | XP_016867486.1:p.Arg104Cys | |
| NM_000168.6:c.313C>T MANE Select | NP_000159.3:p.Arg105Cys |