HGVS | Genome Assembly |
---|---|
NC_000023.11:g.119930108A>C , CM000685.2:g.119930108A>C | GRCh38 |
NC_000023.10:g.119064071A>C , CM000685.1:g.119064071A>C | GRCh37 |
NC_000023.9:g.118948099A>C | NCBI36 |
NG_021260.1:g.18665T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371410.5:c.981T>G MANE Select | ENSP00000360464.3:p.Ala327= | |
ENST00000652253.1:c.977T>G | ||
ENST00000371410.4:c.981T>G | ENSP00000360464.3:p.Ala327= | |
ENST00000477789.5:n.1909T>G | ||
NM_024528.3:c.981T>G | NP_078804.2:p.Ala327= | |
XM_017029842.1:c.684T>G | XP_016885331.1:p.Ala228= | |
NM_024528.4:c.981T>G MANE Select | NP_078804.2:p.Ala327= |