Canonical Allele Identifier: CA1949577528

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254503_5254514delinsACAACCAGGAGC , CM000673.2:g.5254503_5254514delinsACAACCAGGAGC	GRCh38
NC_000011.9:g.5275733_5275744delinsACAACCAGGAGC , CM000673.1:g.5275733_5275744delinsACAACCAGGAGC	GRCh37
NC_000011.8:g.5232309_5232320delinsACAACCAGGAGC	NCBI36
NG_000007.3:g.43102_43113delinsGCTCCTGGTTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.93_104delinsGCTCCTGGTTGT MANE Select	ENSP00000338082.4:p.Arg31=
ENST00000380252.6:c.-73_-62delinsGCTCCTGGTTGT	ENSP00000369602.2:n.-73_-62delinsGCTCCTGG...
ENST00000380259.7:c.1639_1650delinsGCTCCTGGTTGT	ENSP00000369609.3:n.1639_1650delinsGCTCCT...
ENST00000642908.1:c.93_104delinsGCTCCTGGTTGT	ENSP00000495346.1:p.Arg31=
ENST00000647543.1:c.93_104delinsGCTCCTGGTTGT	ENSP00000496470.1:p.Arg31=
ENST00000336906.4:c.93_104delinsGCTCCTGGTTGT	ENSP00000338082.4:p.Arg31=
ENST00000380252.5:c.63_74delinsGCTCCTGGTTGT	ENSP00000369602.1:p.Arg21=
ENST00000380259.6:c.93_104delinsGCTCCTGGTTGT	ENSP00000369609.2:p.Arg31=
ENST00000444587.1:c.55_66delinsGCTCCTGGTTGT	ENSP00000488218.1:p.Ala19=
ENST00000620888.4:c.93_104delinsGCTCCTGGTTGT	ENSP00000479637.1:p.Arg31=
ENST00000624109.1:c.251_262delinsACAACCAGGAGC	ENSP00000485458.1:p.Asp84=
NM_000184.2:c.93_104delinsGCTCCTGGTTGT	NP_000175.1:p.Arg31=
NM_000184.3:c.93_104delinsGCTCCTGGTTGT MANE Select	NP_000175.1:p.Arg31=