HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672409C>G , CM000672.2:g.119672409C>G | GRCh38 |
NC_000010.10:g.121431921C>G , CM000672.1:g.121431921C>G | GRCh37 |
NC_000010.9:g.121421911C>G | NCBI36 |
NG_016125.1:g.26040C>G , LRG_742:g.26040C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369085.8:c.662C>G MANE Select | ENSP00000358081.4:p.Ala221Gly | |
ENST00000369085.7:c.662C>G | ENSP00000358081.3:p.Ala221Gly | |
ENST00000450186.1:c.488C>G | ENSP00000410036.1:p.Ala163Gly | |
NM_004281.3:c.662C>G , LRG_742t1:c.662C>G | NP_004272.2:p.Ala221Gly | |
XM_005270287.1:c.662C>G | XP_005270344.1:p.Ala221Gly | |
XM_005270287.2:c.662C>G | XP_005270344.1:p.Ala221Gly | |
NM_004281.4:c.662C>G MANE Select | NP_004272.2:p.Ala221Gly |