Canonical Allele Identifier: CA918809773
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1554921790

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250079del , CM000673.2:g.5250079del GRCh38
NC_000011.9:g.5271309del , CM000673.1:g.5271309del GRCh37
NC_000011.8:g.5227885del NCBI36
NG_000007.3:g.47537del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1592del ENSP00000495346.1:n.316-1592del
ENST00000647543.1:c.379-1592del ENSP00000496470.1:n.379-1592del
ENST00000620888.4:c.316-1592del ENSP00000479637.1:n.316-1592del