Canonical Allele Identifier: CA124626
Gene: HBG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15033
ClinVar RCV Id: RCV001814967
dbSNP Id: rs35983258
gnomAD v2: 11-5271283-G-A
gnomAD v3: 11-5250053-G-A
gnomAD v4: 11-5250053-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250053G>A , CM000673.2:g.5250053G>A GRCh38
NC_000011.9:g.5271283G>A , CM000673.1:g.5271283G>A GRCh37
NC_000011.8:g.5227859G>A NCBI36
NG_000007.3:g.47563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1566C>T ENSP00000495346.1:n.316-1566C>T
ENST00000647543.1:c.379-1566C>T ENSP00000496470.1:n.379-1566C>T
ENST00000620888.4:c.316-1566C>T ENSP00000479637.1:n.316-1566C>T