Canonical Allele Identifier: CA1949584422
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250068G= , CM000673.2:g.5250068G= GRCh38
NC_000011.9:g.5271298G= , CM000673.1:g.5271298G= GRCh37
NC_000011.8:g.5227874G= NCBI36
NG_000007.3:g.47548C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642908.1:c.316-1581C= ENSP00000495346.1:n.316-1581C=
ENST00000647543.1:c.379-1581C= ENSP00000496470.1:n.379-1581C=
ENST00000620888.4:c.316-1581C= ENSP00000479637.1:n.316-1581C=