HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29534230C>G , CM000679.2:g.29534230C>G | GRCh38 |
NC_000017.10:g.27861248C>G , CM000679.1:g.27861248C>G | GRCh37 |
NC_000017.9:g.24885374C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261716.8:c.2474C>G MANE Select | ENSP00000261716.3:p.Ala825Gly | |
ENST00000261716.7:c.2474C>G | ENSP00000261716.3:p.Ala825Gly | |
ENST00000536202.1:c.2030C>G | ENSP00000438819.1:p.Ala677Gly | |
NM_020791.2:c.2474C>G | NP_065842.1:p.Ala825Gly | |
NM_025142.1:c.2030C>G | NP_079418.1:p.Ala677Gly | |
XM_011525060.1:c.2474C>G | XP_011523362.1:p.Ala825Gly | |
XM_011525060.2:c.2474C>G | XP_011523362.1:p.Ala825Gly | |
NM_020791.4:c.2474C>G MANE Select | NP_065842.1:p.Ala825Gly |