Canonical Allele Identifier: CA2579829738
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249936A= , CM000673.2:g.5249936A= GRCh38
NC_000011.9:g.5271166A= , CM000673.1:g.5271166A= GRCh37
NC_000011.8:g.5227742A= NCBI36
NG_000007.3:g.47680T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1449T= ENSP00000495346.1:n.316-1449T=
ENST00000647543.1:c.379-1449T= ENSP00000496470.1:n.379-1449T=
ENST00000620888.4:c.316-1449T= ENSP00000479637.1:n.316-1449T=