Canonical Allele Identifier: CA2612151346

Gene: HBG2

Linked Data

• gnomAD v4: 11-5253217-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253217T>A , CM000673.2:g.5253217T>A	GRCh38
NC_000011.9:g.5274447T>A , CM000673.1:g.5274447T>A	GRCh37
NC_000011.8:g.5231023T>A	NCBI36
NG_000007.3:g.44399A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.*60A>T MANE Select	ENSP00000338082.4:n.*60A>T
ENST00000380252.6:c.*60A>T	ENSP00000369602.2:n.*60A>T
ENST00000642908.1:c.315+1075A>T	ENSP00000495346.1:n.315+1075A>T
ENST00000647543.1:c.378+126A>T	ENSP00000496470.1:n.378+126A>T
ENST00000336906.4:c.*60A>T	ENSP00000338082.4:n.*60A>T
ENST00000380252.5:c.*60A>T	ENSP00000369602.1:n.*60A>T
ENST00000380259.6:c.*60A>T	ENSP00000369609.2:n.*60A>T
ENST00000620888.4:c.315+1075A>T	ENSP00000479637.1:n.315+1075A>T
NM_000184.2:c.*60A>T	NP_000175.1:n.*60A>T
NM_000184.3:c.*60A>T MANE Select	NP_000175.1:n.*60A>T