Canonical Allele Identifier: CA393993219

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223123G>A (hg19) ; chr16:g.173124G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173124G>A , CM000678.2:g.173124G>A	GRCh38
NC_000016.9:g.223123G>A , CM000678.1:g.223123G>A	GRCh37
NC_000016.8:g.163123G>A	NCBI36
NG_000006.1:g.33987G>A
NG_059186.1:g.1474G>A
NG_059271.1:g.5278G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.96-1G>A MANE Select	ENSP00000251595.6:n.96-1G>A
ENST00000251595.10:c.96-1G>A	ENSP00000251595.6:n.96-1G>A
ENST00000397806.1:c.-1-1G>A	ENSP00000380908.1:n.-1-1G>A
ENST00000482565.1:n.231G>A
ENST00000484216.1:n.65-1G>A
NM_000517.4:c.96-1G>A	NP_000508.1:n.96-1G>A
NM_000517.6:c.96-1G>A MANE Select	NP_000508.1:n.96-1G>A