Canonical Allele Identifier: CA472633089

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5274516T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253286T>C , CM000673.2:g.5253286T>C	GRCh38
NC_000011.9:g.5274516T>C , CM000673.1:g.5274516T>C	GRCh37
NC_000011.8:g.5231092T>C	NCBI36
NG_000007.3:g.44330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.435A>G MANE Select	ENSP00000338082.4:p.Arg145=
ENST00000380252.6:c.270A>G	ENSP00000369602.2:p.Arg90=
ENST00000642908.1:c.315+1006A>G	ENSP00000495346.1:n.315+1006A>G
ENST00000647543.1:c.378+57A>G	ENSP00000496470.1:n.378+57A>G
ENST00000336906.4:c.435A>G	ENSP00000338082.4:p.Arg145=
ENST00000380252.5:c.405A>G	ENSP00000369602.1:p.Arg135=
ENST00000380259.6:c.435A>G	ENSP00000369609.2:p.Arg145=
ENST00000620888.4:c.315+1006A>G	ENSP00000479637.1:n.315+1006A>G
NM_000184.2:c.435A>G	NP_000175.1:p.Arg145=
NM_000184.3:c.435A>G MANE Select	NP_000175.1:p.Arg145=