Canonical Allele Identifier: CA2841816159

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173341dup , CM000678.2:g.173341dup	GRCh38
NC_000016.9:g.223340dup , CM000678.1:g.223340dup	GRCh37
NC_000016.8:g.163340dup	NCBI36
NG_000006.1:g.34204dup
NG_059186.1:g.1691dup
NG_059271.1:g.5495dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.300+12dup MANE Select	ENSP00000251595.6:n.300+12dup
ENST00000251595.10:c.300+12dup	ENSP00000251595.6:n.300+12dup
ENST00000397806.1:c.204+12dup	ENSP00000380908.1:n.204+12dup
ENST00000482565.1:n.436+12dup
ENST00000484216.1:n.281dup
NM_000517.4:c.300+12dup	NP_000508.1:n.300+12dup
NM_000517.6:c.300+12dup MANE Select	NP_000508.1:n.300+12dup