Canonical Allele Identifier: CA1949584327
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1589906656

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249990A>C , CM000673.2:g.5249990A>C GRCh38
NC_000011.9:g.5271220A>C , CM000673.1:g.5271220A>C GRCh37
NC_000011.8:g.5227796A>C NCBI36
NG_000007.3:g.47626T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1503T>G ENSP00000495346.1:n.316-1503T>G
ENST00000647543.1:c.379-1503T>G ENSP00000496470.1:n.379-1503T>G
ENST00000620888.4:c.316-1503T>G ENSP00000479637.1:n.316-1503T>G