HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15192193C>T , CM000681.2:g.15192193C>T | GRCh38 |
NC_000019.9:g.15303004C>T , CM000681.1:g.15303004C>T | GRCh37 |
NC_000019.8:g.15164004C>T | NCBI36 |
NG_009819.1:g.13789G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.446G>A MANE Select | ENSP00000263388.1:p.Gly149Asp | |
ENST00000263388.6:c.446G>A | ENSP00000263388.1:p.Gly149Asp | |
ENST00000601011.1:c.443G>A | ENSP00000473138.1:p.Gly148Asp | |
NM_000435.2:c.446G>A | NP_000426.2:p.Gly149Asp | |
XM_005259924.3:c.446G>A | XP_005259981.1:p.Gly149Asp | |
XM_005259924.4:c.446G>A | XP_005259981.1:p.Gly149Asp | |
NM_000435.3:c.446G>A MANE Select | NP_000426.2:p.Gly149Asp |