Canonical Allele Identifier: CA597205421

Gene: HBG2

Linked Data

• dbSNP Id: rs1246746726
• gnomAD v2: 11-5271337-C-G
• gnomAD v3: 11-5250107-C-G
• gnomAD v4: 11-5250107-C-G
• MyVariant Identifiers: chr11:g.5271337C>G (hg19) ; chr11:g.5250107C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5250107C>G , CM000673.2:g.5250107C>G	GRCh38
NC_000011.9:g.5271337C>G , CM000673.1:g.5271337C>G	GRCh37
NC_000011.8:g.5227913C>G	NCBI36
NG_000007.3:g.47509G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642908.1:c.316-1620G>C	ENSP00000495346.1:n.316-1620G>C
ENST00000647543.1:c.379-1620G>C	ENSP00000496470.1:n.379-1620G>C
ENST00000620888.4:c.316-1620G>C	ENSP00000479637.1:n.316-1620G>C