Canonical Allele Identifier: CA2200880938
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173532_173533delinsGC , CM000678.2:g.173532_173533delinsGC GRCh38
NC_000016.9:g.223531_223532delinsGC , CM000678.1:g.223531_223532delinsGC GRCh37
NC_000016.8:g.163531_163532delinsGC NCBI36
NG_000006.1:g.34395_34396delinsGC
NG_059186.1:g.1882_1883delinsGC
NG_059271.1:g.5686_5687delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.361_362delinsGC MANE Select ENSP00000251595.6:p.Ala121=
ENST00000251595.10:c.361_362delinsGC ENSP00000251595.6:p.Ala121=
ENST00000397806.1:c.265_266delinsGC ENSP00000380908.1:p.Ala89=
ENST00000482565.1:n.497_498delinsGC
NM_000517.4:c.361_362delinsGC NP_000508.1:p.Ala121=
NM_000517.6:c.361_362delinsGC MANE Select NP_000508.1:p.Ala121=