Canonical Allele Identifier: CA1949577551
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5254529A= , CM000673.2:g.5254529A= GRCh38
NC_000011.9:g.5275759A= , CM000673.1:g.5275759A= GRCh37
NC_000011.8:g.5232335A= NCBI36
NG_000007.3:g.43087T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336906.6:c.93-15T= MANE Select ENSP00000338082.4:n.93-15T=
ENST00000380252.6:c.-73-15T= ENSP00000369602.2:n.-73-15T=
ENST00000380259.7:c.1639-15T= ENSP00000369609.3:n.1639-15T=
ENST00000642908.1:c.93-15T= ENSP00000495346.1:n.93-15T=
ENST00000647543.1:c.93-15T= ENSP00000496470.1:n.93-15T=
ENST00000336906.4:c.93-15T= ENSP00000338082.4:n.93-15T=
ENST00000380252.5:c.63-15T= ENSP00000369602.1:n.63-15T=
ENST00000380259.6:c.93-15T= ENSP00000369609.2:n.93-15T=
ENST00000444587.1:c.55-15T= ENSP00000488218.1:n.55-15T=
ENST00000620888.4:c.93-15T= ENSP00000479637.1:n.93-15T=
ENST00000624109.1:c.264+13A= ENSP00000485458.1:n.264+13A=
NM_000184.2:c.93-15T= NP_000175.1:n.93-15T=
NM_000184.3:c.93-15T= MANE Select NP_000175.1:n.93-15T=