HGVS | Genome Assembly |
---|---|
NC_000003.12:g.87259761A>T , CM000665.2:g.87259761A>T | GRCh38 |
NC_000003.11:g.87308911A>T , CM000665.1:g.87308911A>T | GRCh37 |
NC_000003.10:g.87391601A>T | NCBI36 |
NG_008225.2:g.21827T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344265.8:c.*133T>A | ENSP00000342931.3:n.*133T>A | |
ENST00000350375.7:c.*133T>A MANE Select | ENSP00000263781.2:n.*133T>A | |
ENST00000344265.7:c.*133T>A | ENSP00000342931.3:n.*133T>A | |
ENST00000350375.6:c.*133T>A | ENSP00000263781.2:n.*133T>A | |
NM_000306.3:c.*133T>A | NP_000297.1:n.*133T>A | |
NM_001122757.2:c.*133T>A | NP_001116229.1:n.*133T>A | |
NM_000306.4:c.*133T>A MANE Select | NP_000297.1:n.*133T>A | |
NM_001122757.3:c.*133T>A | NP_001116229.1:n.*133T>A |