Canonical Allele Identifier: CA1949583881

Gene: HBG1 HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249695C= , CM000673.2:g.5249695C=	GRCh38
NC_000011.9:g.5270925C= , CM000673.1:g.5270925C=	GRCh37
NC_000011.8:g.5227501C=	NCBI36
NG_000007.3:g.47921G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.92+18G= (HBG1) MANE Select	ENSP00000327431.4:n.92+18G=
ENST00000642908.1:c.316-1208G=	ENSP00000495346.1:n.316-1208G=
ENST00000647543.1:c.379-1208G=	ENSP00000496470.1:n.379-1208G=
ENST00000648735.1:n.143+18G= (HBG1)
ENST00000330597.3:c.92+18G= (HBG1)	ENSP00000327431.3:n.92+18G=
ENST00000620888.4:c.316-1208G= (HBG2)	ENSP00000479637.1:n.316-1208G=
ENST00000623781.1:c.265-17C=	ENSP00000485381.1:n.265-17C=
ENST00000632727.1:c.54+56G= (HBG1)	ENSP00000488759.1:n.54+56G=
NM_000559.2:c.92+18G= (HBG1)	NP_000550.2:n.92+18G=
NM_000559.3:c.92+18G= (HBG1) MANE Select	NP_000550.2:n.92+18G=