Canonical Allele Identifier: CA1949563866

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225539T= , CM000673.2:g.5225539T=	GRCh38
NC_000011.9:g.5246769T= , CM000673.1:g.5246769T=	GRCh37
NC_000011.8:g.5203345T=	NCBI36
NG_000007.3:g.72077A=
NG_059281.1:g.6533A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.*59A=	ENSP00000494175.1:n.*59A=
ENST00000335295.4:c.*59A= MANE Select	ENSP00000333994.3:n.*59A=
ENST00000633227.1:c.*319A=	ENSP00000488004.1:n.*319A=
NM_000518.4:c.*59A=	NP_000509.1:n.*59A=
NM_000518.5:c.*59A= MANE Select	NP_000509.1:n.*59A=