Canonical Allele Identifier: CA2200880632
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173138T= , CM000678.2:g.173138T= GRCh38
NC_000016.9:g.223137T= , CM000678.1:g.223137T= GRCh37
NC_000016.8:g.163137T= NCBI36
NG_000006.1:g.34001T=
NG_059186.1:g.1488T=
NG_059271.1:g.5292T=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.109T= MANE Select ENSP00000251595.6:p.Phe37=
ENST00000251595.10:c.109T= ENSP00000251595.6:p.Phe37=
ENST00000397806.1:c.13T= ENSP00000380908.1:p.Phe5=
ENST00000482565.1:n.245T=
ENST00000484216.1:n.78T=
NM_000517.4:c.109T= NP_000508.1:p.Phe37=
NM_000517.6:c.109T= MANE Select NP_000508.1:p.Phe37=