Canonical Allele Identifier: CA1949584250
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1847927301

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249942_5249947del , CM000673.2:g.5249942_5249947del GRCh38
NC_000011.9:g.5271172_5271177del , CM000673.1:g.5271172_5271177del GRCh37
NC_000011.8:g.5227748_5227753del NCBI36
NG_000007.3:g.47669_47674del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1460_316-1455del ENSP00000495346.1:n.316-1460_316-1455del
ENST00000647543.1:c.379-1460_379-1455del ENSP00000496470.1:n.379-1460_379-1455del
ENST00000620888.4:c.316-1460_316-1455del ENSP00000479637.1:n.316-1460_316-1455del