HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31531465G= , CM000664.2:g.31531465G= | GRCh38 |
NC_000002.11:g.31756535G= , CM000664.1:g.31756535G= | GRCh37 |
NC_000002.10:g.31610039G= | NCBI36 |
NG_008365.1:g.54507C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622030.2:c.453C= MANE Select | ENSP00000477587.1:p.Phe151= | |
ENST00000622030.1:c.453C= | ENSP00000477587.1:p.Phe151= | |
NM_000348.3:c.453C= | NP_000339.2:p.Phe151= | |
XM_011533069.1:c.231C= | XP_011531371.1:p.Phe77= | |
XM_011533070.1:c.198C= | XP_011531372.1:p.Phe66= | |
XM_011533071.1:c.198C= | XP_011531373.1:p.Phe66= | |
XM_011533072.1:c.198C= | XP_011531374.1:p.Phe66= | |
XM_011533069.2:c.231C= | XP_011531371.1:p.Phe77= | |
XM_011533072.2:c.198C= | XP_011531374.1:p.Phe66= | |
NM_000348.4:c.453C= MANE Select | NP_000339.2:p.Phe151= |