Canonical Allele Identifier: CA2200880696
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173216_173258delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA , CM000678.2:g.173216_173258delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA GRCh38
NC_000016.9:g.223215_223257delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA , CM000678.1:g.223215_223257delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA GRCh37
NC_000016.8:g.163215_163257delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA NCBI36
NG_000006.1:g.34079_34121delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA
NG_059186.1:g.1566_1608delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA
NG_059271.1:g.5370_5412delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.187_229delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA MANE Select ENSP00000251595.6:p.Val63=
ENST00000251595.10:c.187_229delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA ENSP00000251595.6:p.Val63=
ENST00000397806.1:c.91_133delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA ENSP00000380908.1:p.Val31=
ENST00000482565.1:n.323_365delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA
ENST00000484216.1:n.156_198delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA
NM_000517.4:c.187_229delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA NP_000508.1:p.Val63=
NM_000517.6:c.187_229delinsGTGGCCGACGCGCTGACCAACGCCGTGGCGCACGTGGACGACA MANE Select NP_000508.1:p.Val63=