HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125489C= , CM000666.2:g.55125489C= | GRCh38 |
NC_000004.11:g.55991656C= , CM000666.1:g.55991656C= | GRCh37 |
NC_000004.10:g.55686413C= | NCBI36 |
NG_012004.1:g.5107G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-196G= MANE Select | ENSP00000263923.4:n.-196G= | |
ENST00000263923.4:c.-196G= | ENSP00000263923.4:n.-196G= | |
NM_002253.2:c.-196G= | NP_002244.1:n.-196G= | |
NM_002253.3:c.-196G= | NP_002244.1:n.-196G= | |
NM_002253.4:c.-196G= MANE Select | NP_002244.1:n.-196G= |