Canonical Allele Identifier: CA1949577535
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5254507C= , CM000673.2:g.5254507C= GRCh38
NC_000011.9:g.5275737C= , CM000673.1:g.5275737C= GRCh37
NC_000011.8:g.5232313C= NCBI36
NG_000007.3:g.43109G=

Transcript Alleles

HGVS Amino-acid change
ENST00000336906.6:c.100G= MANE Select ENSP00000338082.4:p.Val34=
ENST00000380252.6:c.-66G= ENSP00000369602.2:n.-66G=
ENST00000380259.7:c.1646G= ENSP00000369609.3:n.1646G=
ENST00000642908.1:c.100G= ENSP00000495346.1:p.Val34=
ENST00000647543.1:c.100G= ENSP00000496470.1:p.Val34=
ENST00000336906.4:c.100G= ENSP00000338082.4:p.Val34=
ENST00000380252.5:c.70G= ENSP00000369602.1:p.Val24=
ENST00000380259.6:c.100G= ENSP00000369609.2:p.Val34=
ENST00000444587.1:c.62G= ENSP00000488218.1:p.Gly21=
ENST00000620888.4:c.100G= ENSP00000479637.1:p.Val34=
ENST00000624109.1:c.255C= ENSP00000485458.1:p.Asn85=
NM_000184.2:c.100G= NP_000175.1:p.Val34=
NM_000184.3:c.100G= MANE Select NP_000175.1:p.Val34=