Canonical Allele Identifier: CA1949567419
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226588C= , CM000673.2:g.5226588C= GRCh38
NC_000011.9:g.5247818C= , CM000673.1:g.5247818C= GRCh37
NC_000011.8:g.5204394C= NCBI36
NG_000007.3:g.71028G=
NG_059281.1:g.5484G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.304G= ENSP00000494175.1:p.Glu102=
ENST00000335295.4:c.304G= MANE Select ENSP00000333994.3:p.Glu102=
ENST00000475226.1:n.236G=
ENST00000485743.1:n.355G=
ENST00000633227.1:c.*120G= ENSP00000488004.1:n.*120G=
NM_000518.4:c.304G= NP_000509.1:p.Glu102=
NM_000518.5:c.304G= MANE Select NP_000509.1:p.Glu102=