Canonical Allele Identifier: CA379264657

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275715C>G (hg19) ; chr11:g.5254485C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254485C>G , CM000673.2:g.5254485C>G	GRCh38
NC_000011.9:g.5275715C>G , CM000673.1:g.5275715C>G	GRCh37
NC_000011.8:g.5232291C>G	NCBI36
NG_000007.3:g.43131G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.122G>C MANE Select	ENSP00000338082.4:p.Arg41Thr
ENST00000380252.6:c.-44G>C	ENSP00000369602.2:n.-44G>C
ENST00000380259.7:c.1668G>C	ENSP00000369609.3:n.1668G>C
ENST00000642908.1:c.122G>C	ENSP00000495346.1:p.Arg41Thr
ENST00000647543.1:c.122G>C	ENSP00000496470.1:p.Arg41Thr
ENST00000336906.4:c.122G>C	ENSP00000338082.4:p.Arg41Thr
ENST00000380252.5:c.92G>C	ENSP00000369602.1:p.Arg31Thr
ENST00000380259.6:c.122G>C	ENSP00000369609.2:p.Arg41Thr
ENST00000444587.1:c.84G>C	ENSP00000488218.1:p.Glu28Asp
ENST00000620888.4:c.122G>C	ENSP00000479637.1:p.Arg41Thr
ENST00000624109.1:c.233C>G	ENSP00000485458.1:p.Pro78Arg
NM_000184.2:c.122G>C	NP_000175.1:p.Arg41Thr
NM_000184.3:c.122G>C MANE Select	NP_000175.1:p.Arg41Thr