HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429784T>A , CM000663.2:g.68429784T>A | GRCh38 |
NC_000001.10:g.68895467T>A , CM000663.1:g.68895467T>A | GRCh37 |
NC_000001.9:g.68668055T>A | NCBI36 |
NG_008472.1:g.25176A>T | |
NG_008472.2:g.25176A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1594A>T MANE Select | ENSP00000262340.5:p.Lys532Ter | |
ENST00000262340.5:c.1594A>T | ENSP00000262340.5:p.Lys532Ter | |
NM_000329.2:c.1594A>T | NP_000320.1:p.Lys532Ter | |
XM_017002027.1:c.1318A>T | XP_016857516.1:p.Lys440Ter | |
NM_000329.3:c.1594A>T MANE Select | NP_000320.1:p.Lys532Ter |