Canonical Allele Identifier: CA1949565738
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225838T= , CM000673.2:g.5225838T= GRCh38
NC_000011.9:g.5247068T= , CM000673.1:g.5247068T= GRCh37
NC_000011.8:g.5203644T= NCBI36
NG_000007.3:g.71778A=
NG_059281.1:g.6234A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.316-112A= ENSP00000494175.1:n.316-112A=
ENST00000335295.4:c.316-112A= MANE Select ENSP00000333994.3:n.316-112A=
ENST00000475226.1:n.248-112A=
ENST00000633227.1:c.*132-112A= ENSP00000488004.1:n.*132-112A=
NM_000518.4:c.316-112A= NP_000509.1:n.316-112A=
NM_000518.5:c.316-112A= MANE Select NP_000509.1:n.316-112A=