Canonical Allele Identifier: CA379265772

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5276004G>C (hg19) ; chr11:g.5254774G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254774G>C , CM000673.2:g.5254774G>C	GRCh38
NC_000011.9:g.5276004G>C , CM000673.1:g.5276004G>C	GRCh37
NC_000011.8:g.5232580G>C	NCBI36
NG_000007.3:g.42842C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.-46C>G MANE Select	ENSP00000338082.4:n.-46C>G
ENST00000380252.6:c.-73-260C>G	ENSP00000369602.2:n.-73-260C>G
ENST00000380259.7:c.1501C>G	ENSP00000369609.3:n.1501C>G
ENST00000642908.1:c.-46C>G	ENSP00000495346.1:n.-46C>G
ENST00000647543.1:c.-46C>G	ENSP00000496470.1:n.-46C>G
ENST00000336906.4:c.-46C>G	ENSP00000338082.4:n.-46C>G
ENST00000380252.5:c.63-260C>G	ENSP00000369602.1:n.63-260C>G
ENST00000380259.6:c.-46C>G	ENSP00000369609.2:n.-46C>G
ENST00000620888.4:c.-46C>G	ENSP00000479637.1:n.-46C>G
ENST00000624109.1:c.403G>C	ENSP00000485458.1:p.Ala135Pro
NM_000184.2:c.-46C>G	NP_000175.1:n.-46C>G
NM_000184.3:c.-46C>G MANE Select	NP_000175.1:n.-46C>G