Canonical Allele Identifier: CA1949587822
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5253180G= , CM000673.2:g.5253180G= GRCh38
NC_000011.9:g.5274410G= , CM000673.1:g.5274410G= GRCh37
NC_000011.8:g.5230986G= NCBI36
NG_000007.3:g.44436C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.315+1112C= ENSP00000495346.1:n.315+1112C=
ENST00000647543.1:c.378+163C= ENSP00000496470.1:n.378+163C=
ENST00000620888.4:c.315+1112C= ENSP00000479637.1:n.315+1112C=