Canonical Allele Identifier: CA379264994

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275879T>A (hg19) ; chr11:g.5254649T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254649T>A , CM000673.2:g.5254649T>A	GRCh38
NC_000011.9:g.5275879T>A , CM000673.1:g.5275879T>A	GRCh37
NC_000011.8:g.5232455T>A	NCBI36
NG_000007.3:g.42967A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.80A>T MANE Select	ENSP00000338082.4:p.Glu27Val
ENST00000380252.6:c.-73-135A>T	ENSP00000369602.2:n.-73-135A>T
ENST00000380259.7:c.1626A>T	ENSP00000369609.3:n.1626A>T
ENST00000642908.1:c.80A>T	ENSP00000495346.1:p.Glu27Val
ENST00000647543.1:c.80A>T	ENSP00000496470.1:p.Glu27Val
ENST00000336906.4:c.80A>T	ENSP00000338082.4:p.Glu27Val
ENST00000380252.5:c.63-135A>T	ENSP00000369602.1:n.63-135A>T
ENST00000380259.6:c.80A>T	ENSP00000369609.2:p.Glu27Val
ENST00000444587.1:c.54+26A>T	ENSP00000488218.1:n.54+26A>T
ENST00000620888.4:c.80A>T	ENSP00000479637.1:p.Glu27Val
ENST00000624109.1:c.278T>A	ENSP00000485458.1:p.Phe93Tyr
NM_000184.2:c.80A>T	NP_000175.1:p.Glu27Val
NM_000184.3:c.80A>T MANE Select	NP_000175.1:p.Glu27Val