Canonical Allele Identifier: CA2200880747
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173285G= , CM000678.2:g.173285G= GRCh38
NC_000016.9:g.223284G= , CM000678.1:g.223284G= GRCh37
NC_000016.8:g.163284G= NCBI36
NG_000006.1:g.34148G=
NG_059186.1:g.1635G=
NG_059271.1:g.5439G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.256G= MANE Select ENSP00000251595.6:p.Asp86=
ENST00000251595.10:c.256G= ENSP00000251595.6:p.Asp86=
ENST00000397806.1:c.160G= ENSP00000380908.1:p.Asp54=
ENST00000482565.1:n.392G=
ENST00000484216.1:n.225G=
NM_000517.4:c.256G= NP_000508.1:p.Asp86=
NM_000517.6:c.256G= MANE Select NP_000508.1:p.Asp86=