Canonical Allele Identifier: CA217120538

Gene: HBG2

Linked Data

• dbSNP Id: rs748568936
• MyVariant Identifiers: chr11:g.5274502T>G (hg19) ; chr11:g.5253272T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253272T>G , CM000673.2:g.5253272T>G	GRCh38
NC_000011.9:g.5274502T>G , CM000673.1:g.5274502T>G	GRCh37
NC_000011.8:g.5231078T>G	NCBI36
NG_000007.3:g.44344A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.*5A>C MANE Select	ENSP00000338082.4:n.*5A>C
ENST00000380252.6:c.*5A>C	ENSP00000369602.2:n.*5A>C
ENST00000642908.1:c.315+1020A>C	ENSP00000495346.1:n.315+1020A>C
ENST00000647543.1:c.378+71A>C	ENSP00000496470.1:n.378+71A>C
ENST00000336906.4:c.*5A>C	ENSP00000338082.4:n.*5A>C
ENST00000380252.5:c.*5A>C	ENSP00000369602.1:n.*5A>C
ENST00000380259.6:c.*5A>C	ENSP00000369609.2:n.*5A>C
ENST00000620888.4:c.315+1020A>C	ENSP00000479637.1:n.315+1020A>C
NM_000184.2:c.*5A>C	NP_000175.1:n.*5A>C
NM_000184.3:c.*5A>C MANE Select	NP_000175.1:n.*5A>C