HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125442C= , CM000666.2:g.55125442C= | GRCh38 |
NC_000004.11:g.55991609C= , CM000666.1:g.55991609C= | GRCh37 |
NC_000004.10:g.55686366C= | NCBI36 |
NG_012004.1:g.5154G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-149G= MANE Select | ENSP00000263923.4:n.-149G= | |
ENST00000263923.4:c.-149G= | ENSP00000263923.4:n.-149G= | |
NM_002253.2:c.-149G= | NP_002244.1:n.-149G= | |
NM_002253.3:c.-149G= | NP_002244.1:n.-149G= | |
NM_002253.4:c.-149G= MANE Select | NP_002244.1:n.-149G= |