Canonical Allele Identifier: CA2200880503
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173005G= , CM000678.2:g.173005G= GRCh38
NC_000016.9:g.223004G= , CM000678.1:g.223004G= GRCh37
NC_000016.8:g.163004G= NCBI36
NG_000006.1:g.33868G=
NG_059186.1:g.1355G=
NG_059271.1:g.5159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.93G= MANE Select ENSP00000251595.6:p.Glu31=
ENST00000251595.10:c.93G= ENSP00000251595.6:p.Glu31=
ENST00000397806.1:c.-2+47G= ENSP00000380908.1:n.-2+47G=
ENST00000482565.1:n.112G=
ENST00000484216.1:n.62G=
NM_000517.4:c.93G= NP_000508.1:p.Glu31=
NM_000517.6:c.93G= MANE Select NP_000508.1:p.Glu31=