HGVS | Genome Assembly |
---|---|
NC_000001.11:g.205669127C= , CM000663.2:g.205669127C= | GRCh38 |
NC_000001.10:g.205638255C= , CM000663.1:g.205638255C= | GRCh37 |
NC_000001.9:g.203904878C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367145.4:c.-230-4241G= MANE Select | ENSP00000356113.3:n.-230-4241G= | |
ENST00000367145.3:c.-230-4241G= | ENSP00000356113.3:n.-230-4241G= | |
NM_033102.2:c.-230-4241G= | NP_149093.1:n.-230-4241G= | |
XM_005245556.2:c.-231+568G= | XP_005245613.1:n.-231+568G= | |
XM_005245557.3:c.-230-4241G= | XP_005245614.1:n.-230-4241G= | |
XM_005245559.3:c.-231+2823G= | XP_005245616.1:n.-231+2823G= | |
XM_005245560.2:c.-230-4241G= | XP_005245617.1:n.-230-4241G= | |
NM_033102.3:c.-230-4241G= MANE Select | NP_149093.1:n.-230-4241G= |