Canonical Allele Identifier: CA472633862

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275563G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254333G>A , CM000673.2:g.5254333G>A	GRCh38
NC_000011.9:g.5275563G>A , CM000673.1:g.5275563G>A	GRCh37
NC_000011.8:g.5232139G>A	NCBI36
NG_000007.3:g.43283C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.274C>T MANE Select	ENSP00000338082.4:p.Leu92=
ENST00000380252.6:c.109C>T	ENSP00000369602.2:p.Leu37=
ENST00000642908.1:c.274C>T	ENSP00000495346.1:p.Leu92=
ENST00000647543.1:c.274C>T	ENSP00000496470.1:p.Leu92=
ENST00000336906.4:c.274C>T	ENSP00000338082.4:p.Leu92=
ENST00000380252.5:c.244C>T	ENSP00000369602.1:p.Leu82=
ENST00000380259.6:c.274C>T	ENSP00000369609.2:p.Leu92=
ENST00000444587.1:c.*143C>T	ENSP00000488218.1:n.*143C>T
ENST00000620888.4:c.274C>T	ENSP00000479637.1:p.Leu92=
ENST00000624109.1:c.81G>A	ENSP00000485458.1:p.Gln27=
NM_000184.2:c.274C>T	NP_000175.1:p.Leu92=
NM_000184.3:c.274C>T MANE Select	NP_000175.1:p.Leu92=