Canonical Allele Identifier: CA1949565737
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225835G= , CM000673.2:g.5225835G= GRCh38
NC_000011.9:g.5247065G= , CM000673.1:g.5247065G= GRCh37
NC_000011.8:g.5203641G= NCBI36
NG_000007.3:g.71781C=
NG_059281.1:g.6237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.316-109C= ENSP00000494175.1:n.316-109C=
ENST00000335295.4:c.316-109C= MANE Select ENSP00000333994.3:n.316-109C=
ENST00000475226.1:n.248-109C=
ENST00000633227.1:c.*132-109C= ENSP00000488004.1:n.*132-109C=
NM_000518.4:c.316-109C= NP_000509.1:n.316-109C=
NM_000518.5:c.316-109C= MANE Select NP_000509.1:n.316-109C=