HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125564T= , CM000666.2:g.55125564T= | GRCh38 |
NC_000004.11:g.55991731T= , CM000666.1:g.55991731T= | GRCh37 |
NC_000004.10:g.55686488T= | NCBI36 |
NG_012004.1:g.5032A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-271A= MANE Select | ENSP00000263923.4:n.-271A= | |
ENST00000263923.4:c.-271A= | ENSP00000263923.4:n.-271A= | |
NM_002253.2:c.-271A= | NP_002244.1:n.-271A= | |
NM_002253.3:c.-271A= | NP_002244.1:n.-271A= | |
NM_002253.4:c.-271A= MANE Select | NP_002244.1:n.-271A= |