Canonical Allele Identifier: CA1949584413
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250060G= , CM000673.2:g.5250060G= GRCh38
NC_000011.9:g.5271290G= , CM000673.1:g.5271290G= GRCh37
NC_000011.8:g.5227866G= NCBI36
NG_000007.3:g.47556C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1573C= ENSP00000495346.1:n.316-1573C=
ENST00000647543.1:c.379-1573C= ENSP00000496470.1:n.379-1573C=
ENST00000620888.4:c.316-1573C= ENSP00000479637.1:n.316-1573C=