Canonical Allele Identifier: CA2841816160

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173346dup , CM000678.2:g.173346dup	GRCh38
NC_000016.9:g.223345dup , CM000678.1:g.223345dup	GRCh37
NC_000016.8:g.163345dup	NCBI36
NG_000006.1:g.34209dup
NG_059186.1:g.1696dup
NG_059271.1:g.5500dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.300+17dup MANE Select	ENSP00000251595.6:n.300+17dup
ENST00000251595.10:c.300+17dup	ENSP00000251595.6:n.300+17dup
ENST00000397806.1:c.204+17dup	ENSP00000380908.1:n.204+17dup
ENST00000482565.1:n.436+17dup
ENST00000484216.1:n.286dup
NM_000517.4:c.300+17dup	NP_000508.1:n.300+17dup
NM_000517.6:c.300+17dup MANE Select	NP_000508.1:n.300+17dup