HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119676532C>A , CM000672.2:g.119676532C>A | GRCh38 |
NC_000010.10:g.121436044C>A , CM000672.1:g.121436044C>A | GRCh37 |
NC_000010.9:g.121426034C>A | NCBI36 |
NG_016125.1:g.30163C>A , LRG_742:g.30163C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369085.8:c.978C>A MANE Select | ENSP00000358081.4:p.Gly326= | |
ENST00000369085.7:c.978C>A | ENSP00000358081.3:p.Gly326= | |
ENST00000450186.1:c.801C>A | ENSP00000410036.1:p.Gly267= | |
NM_004281.3:c.978C>A , LRG_742t1:c.978C>A | NP_004272.2:p.Gly326= | |
XM_005270287.1:c.975C>A | XP_005270344.1:p.Gly325= | |
XM_005270287.2:c.975C>A | XP_005270344.1:p.Gly325= | |
NM_004281.4:c.978C>A MANE Select | NP_004272.2:p.Gly326= |