Canonical Allele Identifier: CA2200880701
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173223A= , CM000678.2:g.173223A= GRCh38
NC_000016.9:g.223222A= , CM000678.1:g.223222A= GRCh37
NC_000016.8:g.163222A= NCBI36
NG_000006.1:g.34086A=
NG_059186.1:g.1573A=
NG_059271.1:g.5377A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.194A= MANE Select ENSP00000251595.6:p.Asp65=
ENST00000251595.10:c.194A= ENSP00000251595.6:p.Asp65=
ENST00000397806.1:c.98A= ENSP00000380908.1:p.Asp33=
ENST00000482565.1:n.330A=
ENST00000484216.1:n.163A=
NM_000517.4:c.194A= NP_000508.1:p.Asp65=
NM_000517.6:c.194A= MANE Select NP_000508.1:p.Asp65=