Canonical Allele Identifier: CA934695763
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1385004818
gnomAD v3: 11-5249956-C-G
gnomAD v4: 11-5249956-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249956C>G , CM000673.2:g.5249956C>G GRCh38
NC_000011.9:g.5271186C>G , CM000673.1:g.5271186C>G GRCh37
NC_000011.8:g.5227762C>G NCBI36
NG_000007.3:g.47660G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1469G>C ENSP00000495346.1:n.316-1469G>C
ENST00000647543.1:c.379-1469G>C ENSP00000496470.1:n.379-1469G>C
ENST00000620888.4:c.316-1469G>C ENSP00000479637.1:n.316-1469G>C