HGVS | Genome Assembly |
---|---|
NC_000005.10:g.33944789C>A , CM000667.2:g.33944789C>A | GRCh38 |
NC_000005.9:g.33944894C>A , CM000667.1:g.33944894C>A | GRCh37 |
NC_000005.8:g.33980651C>A | NCBI36 |
NG_011691.2:g.44887G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296589.9:c.1452G>T MANE Select | ENSP00000296589.4:p.Gln484His | |
ENST00000296589.8:c.1452G>T | ENSP00000296589.4:p.Gln484His | |
NM_016180.4:c.1452G>T | NP_057264.3:p.Gln484His | |
XM_011514051.1:c.1050G>T | XP_011512353.1:p.Gln350His | |
NM_016180.5:c.1452G>T MANE Select | NP_057264.4:p.Gln484His |