Canonical Allele Identifier: CA1949584380
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250050T= , CM000673.2:g.5250050T= GRCh38
NC_000011.9:g.5271280T= , CM000673.1:g.5271280T= GRCh37
NC_000011.8:g.5227856T= NCBI36
NG_000007.3:g.47566A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1563A= ENSP00000495346.1:n.316-1563A=
ENST00000647543.1:c.379-1563A= ENSP00000496470.1:n.379-1563A=
ENST00000620888.4:c.316-1563A= ENSP00000479637.1:n.316-1563A=