HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85581868C= , CM000664.2:g.85581868C= | GRCh38 |
NC_000002.11:g.85808991C= , CM000664.1:g.85808991C= | GRCh37 |
NC_000002.10:g.85662502C= | NCBI36 |
NG_022887.1:g.9378C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263864.10:c.*152C= MANE Select | ENSP00000263864.5:n.*152C= | |
ENST00000263864.9:c.*152C= | ENSP00000263864.5:n.*152C= | |
ENST00000409760.1:c.*288C= | ENSP00000387094.1:n.*288C= | |
ENST00000432071.1:c.*152C= | ENSP00000407984.1:n.*152C= | |
NM_003761.4:c.*152C= | NP_003752.2:n.*152C= | |
XM_017005170.1:c.*288C= | XP_016860659.1:n.*288C= | |
NM_003761.5:c.*152C= MANE Select | NP_003752.2:n.*152C= |