Canonical Allele Identifier: CA2630738106

Gene: HBA2

Linked Data

• gnomAD v4: 16-173668-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173670dup , CM000678.2:g.173670dup	GRCh38
NC_000016.9:g.223669dup , CM000678.1:g.223669dup	GRCh37
NC_000016.8:g.163669dup	NCBI36
NG_000006.1:g.34533dup
NG_059186.1:g.2020dup
NG_059271.1:g.5824dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.*70dup MANE Select	ENSP00000251595.6:n.*70dup
ENST00000251595.10:c.*70dup	ENSP00000251595.6:n.*70dup
ENST00000397806.1:c.*70dup	ENSP00000380908.1:n.*70dup
ENST00000482565.1:n.635dup
NM_000517.4:c.*70dup	NP_000508.1:n.*70dup
NM_000517.6:c.*70dup MANE Select	NP_000508.1:n.*70dup