Canonical Allele Identifier: CA379264327

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275619C>A (hg19) ; chr11:g.5254389C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254389C>A , CM000673.2:g.5254389C>A	GRCh38
NC_000011.9:g.5275619C>A , CM000673.1:g.5275619C>A	GRCh37
NC_000011.8:g.5232195C>A	NCBI36
NG_000007.3:g.43227G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.218G>T MANE Select	ENSP00000338082.4:p.Gly73Val
ENST00000380252.6:c.53G>T	ENSP00000369602.2:p.Gly18Val
ENST00000642908.1:c.218G>T	ENSP00000495346.1:p.Gly73Val
ENST00000647543.1:c.218G>T	ENSP00000496470.1:p.Gly73Val
ENST00000336906.4:c.218G>T	ENSP00000338082.4:p.Gly73Val
ENST00000380252.5:c.188G>T	ENSP00000369602.1:p.Gly63Val
ENST00000380259.6:c.218G>T	ENSP00000369609.2:p.Gly73Val
ENST00000444587.1:c.*87G>T	ENSP00000488218.1:n.*87G>T
ENST00000620888.4:c.218G>T	ENSP00000479637.1:p.Gly73Val
ENST00000624109.1:c.137C>A	ENSP00000485458.1:p.Ser46Tyr
NM_000184.2:c.218G>T	NP_000175.1:p.Gly73Val
NM_000184.3:c.218G>T MANE Select	NP_000175.1:p.Gly73Val