Canonical Allele Identifier: CA597436259

Gene: HBG2

Linked Data

• dbSNP Id: rs1173312680
• gnomAD v2: 11-5275758-A-C
• gnomAD v4: 11-5254528-A-C
• MyVariant Identifiers: chr11:g.5275758A>C (hg19) ; chr11:g.5254528A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254528A>C , CM000673.2:g.5254528A>C	GRCh38
NC_000011.9:g.5275758A>C , CM000673.1:g.5275758A>C	GRCh37
NC_000011.8:g.5232334A>C	NCBI36
NG_000007.3:g.43088T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.93-14T>G MANE Select	ENSP00000338082.4:n.93-14T>G
ENST00000380252.6:c.-73-14T>G	ENSP00000369602.2:n.-73-14T>G
ENST00000380259.7:c.1639-14T>G	ENSP00000369609.3:n.1639-14T>G
ENST00000642908.1:c.93-14T>G	ENSP00000495346.1:n.93-14T>G
ENST00000647543.1:c.93-14T>G	ENSP00000496470.1:n.93-14T>G
ENST00000336906.4:c.93-14T>G	ENSP00000338082.4:n.93-14T>G
ENST00000380252.5:c.63-14T>G	ENSP00000369602.1:n.63-14T>G
ENST00000380259.6:c.93-14T>G	ENSP00000369609.2:n.93-14T>G
ENST00000444587.1:c.55-14T>G	ENSP00000488218.1:n.55-14T>G
ENST00000620888.4:c.93-14T>G	ENSP00000479637.1:n.93-14T>G
ENST00000624109.1:c.264+12A>C	ENSP00000485458.1:n.264+12A>C
NM_000184.2:c.93-14T>G	NP_000175.1:n.93-14T>G
NM_000184.3:c.93-14T>G MANE Select	NP_000175.1:n.93-14T>G