HGVS | Genome Assembly |
---|---|
NC_000002.12:g.102532657G>T , CM000664.2:g.102532657G>T | GRCh38 |
NC_000002.11:g.103149116G>T , CM000664.1:g.103149116G>T | GRCh37 |
NC_000002.10:g.102515548G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295269.5:c.2366G>T MANE Select | ENSP00000295269.4:p.Arg789Met | |
ENST00000295269.4:c.2366G>T | ENSP00000295269.4:p.Arg789Met | |
NM_001011552.3:c.2366G>T | NP_001011552.2:p.Arg789Met | |
XM_011511158.1:c.2279G>T | XP_011509460.1:p.Arg760Met | |
NM_001011552.4:c.2366G>T MANE Select | NP_001011552.2:p.Arg789Met |