Canonical Allele Identifier: CA393992822

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.222914G>A (hg19) ; chr16:g.172915G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172915G>A , CM000678.2:g.172915G>A	GRCh38
NC_000016.9:g.222914G>A , CM000678.1:g.222914G>A	GRCh37
NC_000016.8:g.162914G>A	NCBI36
NG_000006.1:g.33778G>A
NG_059186.1:g.1265G>A
NG_059271.1:g.5069G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.3G>A MANE Select	ENSP00000251595.6:p.Met1Ile
ENST00000251595.10:c.3G>A	ENSP00000251595.6:p.Met1Ile
ENST00000397806.1:c.-45G>A	ENSP00000380908.1:n.-45G>A
ENST00000482565.1:n.22G>A
NM_000517.4:c.3G>A	NP_000508.1:p.Met1Ile
NM_000517.6:c.3G>A MANE Select	NP_000508.1:p.Met1Ile