Canonical Allele Identifier: CA2200880311
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172962A= , CM000678.2:g.172962A= GRCh38
NC_000016.9:g.222961A= , CM000678.1:g.222961A= GRCh37
NC_000016.8:g.162961A= NCBI36
NG_000006.1:g.33825A=
NG_059186.1:g.1312A=
NG_059271.1:g.5116A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.50A= MANE Select ENSP00000251595.6:p.Lys17=
ENST00000251595.10:c.50A= ENSP00000251595.6:p.Lys17=
ENST00000397806.1:c.-2+4A= ENSP00000380908.1:n.-2+4A=
ENST00000482565.1:n.69A=
ENST00000484216.1:n.19A=
NM_000517.4:c.50A= NP_000508.1:p.Lys17=
NM_000517.6:c.50A= MANE Select NP_000508.1:p.Lys17=