HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136673633T>A , CM000671.2:g.136673633T>A | GRCh38 |
NC_000009.11:g.139568085T>A , CM000671.1:g.139568085T>A | GRCh37 |
NC_000009.10:g.138687906T>A | NCBI36 |
NG_008090.1:g.18827A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.*119A>T MANE Select | ENSP00000360761.2:n.*119A>T | |
ENST00000371694.7:c.*119A>T | ENSP00000360759.3:n.*119A>T | |
ENST00000371696.6:c.*119A>T | ENSP00000360761.2:n.*119A>T | |
ENST00000538402.1:c.*119A>T | ENSP00000438919.1:n.*119A>T | |
NM_001012727.1:c.*119A>T | NP_001012745.1:n.*119A>T | |
NM_006412.3:c.*119A>T | NP_006403.2:n.*119A>T | |
NM_006412.4:c.*119A>T MANE Select | NP_006403.2:n.*119A>T | |
NM_001012727.2:c.*119A>T | NP_001012745.1:n.*119A>T |