Canonical Allele Identifier: CA1949577231
Gene: HBG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5254304A= , CM000673.2:g.5254304A= GRCh38
NC_000011.9:g.5275534A= , CM000673.1:g.5275534A= GRCh37
NC_000011.8:g.5232110A= NCBI36
NG_000007.3:g.43312T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336906.6:c.303T= MANE Select ENSP00000338082.4:p.Pro101=
ENST00000380252.6:c.138T= ENSP00000369602.2:p.Pro46=
ENST00000642908.1:c.303T= ENSP00000495346.1:p.Pro101=
ENST00000647543.1:c.303T= ENSP00000496470.1:p.Pro101=
ENST00000336906.4:c.303T= ENSP00000338082.4:p.Pro101=
ENST00000380252.5:c.273T= ENSP00000369602.1:p.Pro91=
ENST00000380259.6:c.303T= ENSP00000369609.2:p.Pro101=
ENST00000444587.1:c.*172T= ENSP00000488218.1:n.*172T=
ENST00000620888.4:c.303T= ENSP00000479637.1:p.Pro101=
ENST00000624109.1:c.52A= ENSP00000485458.1:p.Arg18=
NM_000184.2:c.303T= NP_000175.1:p.Pro101=
NM_000184.3:c.303T= MANE Select NP_000175.1:p.Pro101=