Canonical Allele Identifier: CA1949584329
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1847927801

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249992C>A , CM000673.2:g.5249992C>A GRCh38
NC_000011.9:g.5271222C>A , CM000673.1:g.5271222C>A GRCh37
NC_000011.8:g.5227798C>A NCBI36
NG_000007.3:g.47624G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1505G>T ENSP00000495346.1:n.316-1505G>T
ENST00000647543.1:c.379-1505G>T ENSP00000496470.1:n.379-1505G>T
ENST00000620888.4:c.316-1505G>T ENSP00000479637.1:n.316-1505G>T