Canonical Allele Identifier: CA1949567245
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226571A= , CM000673.2:g.5226571A= GRCh38
NC_000011.9:g.5247801A= , CM000673.1:g.5247801A= GRCh37
NC_000011.8:g.5204377A= NCBI36
NG_000007.3:g.71045T=
NG_059281.1:g.5501T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+6T= ENSP00000494175.1:n.315+6T=
ENST00000335295.4:c.315+6T= MANE Select ENSP00000333994.3:n.315+6T=
ENST00000475226.1:n.247+6T=
ENST00000485743.1:n.372T=
ENST00000633227.1:c.*131+6T= ENSP00000488004.1:n.*131+6T=
NM_000518.4:c.315+6T= NP_000509.1:n.315+6T=
NM_000518.5:c.315+6T= MANE Select NP_000509.1:n.315+6T=