Canonical Allele Identifier: CA1949584310
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1847927680
gnomAD v4: 11-5249981-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249981A>G , CM000673.2:g.5249981A>G GRCh38
NC_000011.9:g.5271211A>G , CM000673.1:g.5271211A>G GRCh37
NC_000011.8:g.5227787A>G NCBI36
NG_000007.3:g.47635T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1494T>C ENSP00000495346.1:n.316-1494T>C
ENST00000647543.1:c.379-1494T>C ENSP00000496470.1:n.379-1494T>C
ENST00000620888.4:c.316-1494T>C ENSP00000479637.1:n.316-1494T>C