HGVS | Genome Assembly |
---|---|
NC_000002.12:g.102532655C= , CM000664.2:g.102532655C= | GRCh38 |
NC_000002.11:g.103149114C= , CM000664.1:g.103149114C= | GRCh37 |
NC_000002.10:g.102515546C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295269.5:c.2364C= MANE Select | ENSP00000295269.4:p.His788= | |
ENST00000295269.4:c.2364C= | ENSP00000295269.4:p.His788= | |
NM_001011552.3:c.2364C= | NP_001011552.2:p.His788= | |
XM_011511158.1:c.2277C= | XP_011509460.1:p.His759= | |
NM_001011552.4:c.2364C= MANE Select | NP_001011552.2:p.His788= |