HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226942T>G , CM000673.2:g.5226942T>G | GRCh38 |
NC_000011.9:g.5248172T>G , CM000673.1:g.5248172T>G | GRCh37 |
NC_000011.8:g.5204748T>G | NCBI36 |
NG_000007.3:g.70674A>C | |
NG_059281.1:g.5130A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.80A>C | ENSP00000494175.1:p.Glu27Ala | |
ENST00000335295.4:c.80A>C MANE Select | ENSP00000333994.3:p.Glu27Ala | |
ENST00000380315.2:c.80A>C | ENSP00000369671.2:p.Glu27Ala | |
ENST00000485743.1:n.131A>C | ||
ENST00000633227.1:c.76+4A>C | ENSP00000488004.1:n.76+4A>C | |
NM_000518.4:c.80A>C | NP_000509.1:p.Glu27Ala | |
NM_000518.5:c.80A>C MANE Select | NP_000509.1:p.Glu27Ala |