Canonical Allele Identifier: CA379264349

Gene: HBG2

Linked Data

• dbSNP Id: rs768094911
• COSMIC: COSM3448575
• MyVariant Identifiers: chr11:g.5275627A>T (hg19) ; chr11:g.5254397A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254397A>T , CM000673.2:g.5254397A>T	GRCh38
NC_000011.9:g.5275627A>T , CM000673.1:g.5275627A>T	GRCh37
NC_000011.8:g.5232203A>T	NCBI36
NG_000007.3:g.43219T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.210T>A MANE Select	ENSP00000338082.4:p.Thr70=
ENST00000380252.6:c.45T>A	ENSP00000369602.2:p.Thr15=
ENST00000380259.7:c.1756T>A	ENSP00000369609.3:n.1756T>A
ENST00000642908.1:c.210T>A	ENSP00000495346.1:p.Thr70=
ENST00000647543.1:c.210T>A	ENSP00000496470.1:p.Thr70=
ENST00000336906.4:c.210T>A	ENSP00000338082.4:p.Thr70=
ENST00000380252.5:c.180T>A	ENSP00000369602.1:p.Thr60=
ENST00000380259.6:c.210T>A	ENSP00000369609.2:p.Thr70=
ENST00000444587.1:c.*79T>A	ENSP00000488218.1:n.*79T>A
ENST00000620888.4:c.210T>A	ENSP00000479637.1:p.Thr70=
ENST00000624109.1:c.145A>T	ENSP00000485458.1:p.Ser49Cys
NM_000184.2:c.210T>A	NP_000175.1:p.Thr70=
NM_000184.3:c.210T>A MANE Select	NP_000175.1:p.Thr70=