Canonical Allele Identifier: CA2579829813

Gene: HBG1 HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249820A= , CM000673.2:g.5249820A=	GRCh38
NC_000011.9:g.5271050A= , CM000673.1:g.5271050A=	GRCh37
NC_000011.8:g.5227626A=	NCBI36
NG_000007.3:g.47796T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.-16T= (HBG1) MANE Select	ENSP00000327431.4:n.-16T=
ENST00000642908.1:c.316-1333T=	ENSP00000495346.1:n.316-1333T=
ENST00000647543.1:c.379-1333T=	ENSP00000496470.1:n.379-1333T=
ENST00000648735.1:n.36T= (HBG1)
ENST00000330597.3:c.-16T= (HBG1)	ENSP00000327431.3:n.-16T=
ENST00000620888.4:c.316-1333T= (HBG2)	ENSP00000479637.1:n.316-1333T=
ENST00000623781.1:c.373A=	ENSP00000485381.1:p.Ser125=
ENST00000632727.1:c.-16T= (HBG1)	ENSP00000488759.1:n.-16T=
NM_000559.2:c.-16T= (HBG1)	NP_000550.2:n.-16T=
NM_000559.3:c.-16T= (HBG1) MANE Select	NP_000550.2:n.-16T=