Canonical Allele Identifier: CA913550890
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1564884876
gnomAD v2: 11-5271288-G-C
gnomAD v3: 11-5250058-G-C
gnomAD v4: 11-5250058-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250058G>C , CM000673.2:g.5250058G>C GRCh38
NC_000011.9:g.5271288G>C , CM000673.1:g.5271288G>C GRCh37
NC_000011.8:g.5227864G>C NCBI36
NG_000007.3:g.47558C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1571C>G ENSP00000495346.1:n.316-1571C>G
ENST00000647543.1:c.379-1571C>G ENSP00000496470.1:n.379-1571C>G
ENST00000620888.4:c.316-1571C>G ENSP00000479637.1:n.316-1571C>G