HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136673585T>A , CM000671.2:g.136673585T>A | GRCh38 |
NC_000009.11:g.139568037T>A , CM000671.1:g.139568037T>A | GRCh37 |
NC_000009.10:g.138687858T>A | NCBI36 |
NG_008090.1:g.18875A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.*167A>T MANE Select | ENSP00000360761.2:n.*167A>T | |
ENST00000371694.7:c.*167A>T | ENSP00000360759.3:n.*167A>T | |
ENST00000371696.6:c.*167A>T | ENSP00000360761.2:n.*167A>T | |
ENST00000538402.1:c.*167A>T | ENSP00000438919.1:n.*167A>T | |
NM_001012727.1:c.*167A>T | NP_001012745.1:n.*167A>T | |
NM_006412.3:c.*167A>T | NP_006403.2:n.*167A>T | |
NM_006412.4:c.*167A>T MANE Select | NP_006403.2:n.*167A>T | |
NM_001012727.2:c.*167A>T | NP_001012745.1:n.*167A>T |