HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125462T>A , CM000666.2:g.55125462T>A | GRCh38 |
NC_000004.11:g.55991629T>A , CM000666.1:g.55991629T>A | GRCh37 |
NC_000004.10:g.55686386T>A | NCBI36 |
NG_012004.1:g.5134A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-169A>T MANE Select | ENSP00000263923.4:n.-169A>T | |
ENST00000263923.4:c.-169A>T | ENSP00000263923.4:n.-169A>T | |
NM_002253.2:c.-169A>T | NP_002244.1:n.-169A>T | |
NM_002253.3:c.-169A>T | NP_002244.1:n.-169A>T | |
NM_002253.4:c.-169A>T MANE Select | NP_002244.1:n.-169A>T |