Canonical Allele Identifier: CA1949587799
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5253159A= , CM000673.2:g.5253159A= GRCh38
NC_000011.9:g.5274389A= , CM000673.1:g.5274389A= GRCh37
NC_000011.8:g.5230965A= NCBI36
NG_000007.3:g.44457T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.315+1133T= ENSP00000495346.1:n.315+1133T=
ENST00000647543.1:c.378+184T= ENSP00000496470.1:n.378+184T=
ENST00000620888.4:c.315+1133T= ENSP00000479637.1:n.315+1133T=