Canonical Allele Identifier: CA653938667

Gene: HBG2

Linked Data

• COSMIC: COSN23022465

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253197dup , CM000673.2:g.5253197dup	GRCh38
NC_000011.9:g.5274427dup , CM000673.1:g.5274427dup	GRCh37
NC_000011.8:g.5231003dup	NCBI36
NG_000007.3:g.44419dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.*80dup MANE Select	ENSP00000338082.4:n.*80dup
ENST00000380252.6:c.*80dup	ENSP00000369602.2:n.*80dup
ENST00000642908.1:c.315+1095dup	ENSP00000495346.1:n.315+1095dup
ENST00000647543.1:c.378+146dup	ENSP00000496470.1:n.378+146dup
ENST00000380252.5:c.*80dup	ENSP00000369602.1:n.*80dup
ENST00000380259.6:c.*80dup	ENSP00000369609.2:n.*80dup
ENST00000620888.4:c.315+1095dup	ENSP00000479637.1:n.315+1095dup
NM_000184.2:c.*80dup	NP_000175.1:n.*80dup
NM_000184.3:c.*80dup MANE Select	NP_000175.1:n.*80dup