Canonical Allele Identifier: CA492994735

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223277C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173278C>A , CM000678.2:g.173278C>A	GRCh38
NC_000016.9:g.223277C>A , CM000678.1:g.223277C>A	GRCh37
NC_000016.8:g.163277C>A	NCBI36
NG_000006.1:g.34141C>A
NG_059186.1:g.1628C>A
NG_059271.1:g.5432C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.249C>A MANE Select	ENSP00000251595.6:p.Ala83=
ENST00000251595.10:c.249C>A	ENSP00000251595.6:p.Ala83=
ENST00000397806.1:c.153C>A	ENSP00000380908.1:p.Ala51=
ENST00000482565.1:n.385C>A
ENST00000484216.1:n.218C>A
NM_000517.4:c.249C>A	NP_000508.1:p.Ala83=
NM_000517.6:c.249C>A MANE Select	NP_000508.1:p.Ala83=