Canonical Allele Identifier: CA1949577187
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5254276C= , CM000673.2:g.5254276C= GRCh38
NC_000011.9:g.5275506C= , CM000673.1:g.5275506C= GRCh37
NC_000011.8:g.5232082C= NCBI36
NG_000007.3:g.43340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336906.6:c.315+16G= MANE Select ENSP00000338082.4:n.315+16G=
ENST00000380252.6:c.150+16G= ENSP00000369602.2:n.150+16G=
ENST00000642908.1:c.315+16G= ENSP00000495346.1:n.315+16G=
ENST00000647543.1:c.315+16G= ENSP00000496470.1:n.315+16G=
ENST00000336906.4:c.315+16G= ENSP00000338082.4:n.315+16G=
ENST00000380252.5:c.285+16G= ENSP00000369602.1:n.285+16G=
ENST00000380259.6:c.315+16G= ENSP00000369609.2:n.315+16G=
ENST00000444587.1:c.*184+16G= ENSP00000488218.1:n.*184+16G=
ENST00000620888.4:c.315+16G= ENSP00000479637.1:n.315+16G=
ENST00000624109.1:c.43-19C= ENSP00000485458.1:n.43-19C=
NM_000184.2:c.315+16G= NP_000175.1:n.315+16G=
NM_000184.3:c.315+16G= MANE Select NP_000175.1:n.315+16G=