Canonical Allele Identifier: CA2579829505

Gene: HBG1 HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249843T>G , CM000673.2:g.5249843T>G	GRCh38
NC_000011.9:g.5271073T>G , CM000673.1:g.5271073T>G	GRCh37
NC_000011.8:g.5227649T>G	NCBI36
NG_000007.3:g.47773A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.-39A>C (HBG1) MANE Select	ENSP00000327431.4:n.-39A>C
ENST00000642908.1:c.316-1356A>C	ENSP00000495346.1:n.316-1356A>C
ENST00000647543.1:c.379-1356A>C	ENSP00000496470.1:n.379-1356A>C
ENST00000648735.1:n.13A>C (HBG1)
ENST00000330597.3:c.-39A>C (HBG1)	ENSP00000327431.3:n.-39A>C
ENST00000620888.4:c.316-1356A>C (HBG2)	ENSP00000479637.1:n.316-1356A>C
ENST00000623781.1:c.396T>G	ENSP00000485381.1:p.Val132=
NM_000559.2:c.-39A>C (HBG1)	NP_000550.2:n.-39A>C
NM_000559.3:c.-39A>C (HBG1) MANE Select	NP_000550.2:n.-39A>C