Canonical Allele Identifier: CA379264065

Gene: HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5275520A>C (hg19) ; chr11:g.5254290A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254290A>C , CM000673.2:g.5254290A>C	GRCh38
NC_000011.9:g.5275520A>C , CM000673.1:g.5275520A>C	GRCh37
NC_000011.8:g.5232096A>C	NCBI36
NG_000007.3:g.43326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.315+2T>G MANE Select	ENSP00000338082.4:n.315+2T>G
ENST00000380252.6:c.150+2T>G	ENSP00000369602.2:n.150+2T>G
ENST00000642908.1:c.315+2T>G	ENSP00000495346.1:n.315+2T>G
ENST00000647543.1:c.315+2T>G	ENSP00000496470.1:n.315+2T>G
ENST00000336906.4:c.315+2T>G	ENSP00000338082.4:n.315+2T>G
ENST00000380252.5:c.285+2T>G	ENSP00000369602.1:n.285+2T>G
ENST00000380259.6:c.315+2T>G	ENSP00000369609.2:n.315+2T>G
ENST00000444587.1:c.*184+2T>G	ENSP00000488218.1:n.*184+2T>G
ENST00000620888.4:c.315+2T>G	ENSP00000479637.1:n.315+2T>G
ENST00000624109.1:c.43-5A>C	ENSP00000485458.1:n.43-5A>C
NM_000184.2:c.315+2T>G	NP_000175.1:n.315+2T>G
NM_000184.3:c.315+2T>G MANE Select	NP_000175.1:n.315+2T>G