Canonical Allele Identifier: CA2843200147

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226516dup , CM000673.2:g.5226516dup	GRCh38
NC_000011.9:g.5247746dup , CM000673.1:g.5247746dup	GRCh37
NC_000011.8:g.5204322dup	NCBI36
NG_000007.3:g.71100dup
NG_059281.1:g.5556dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.315+61dup	ENSP00000494175.1:n.315+61dup
ENST00000335295.4:c.315+61dup MANE Select	ENSP00000333994.3:n.315+61dup
ENST00000475226.1:n.247+61dup
ENST00000485743.1:n.427dup
ENST00000633227.1:c.*131+61dup	ENSP00000488004.1:n.*131+61dup
NM_000518.4:c.315+61dup	NP_000509.1:n.315+61dup
NM_000518.5:c.315+61dup MANE Select	NP_000509.1:n.315+61dup