Canonical Allele Identifier: CA492785599

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223584C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173585C>A , CM000678.2:g.173585C>A	GRCh38
NC_000016.9:g.223584C>A , CM000678.1:g.223584C>A	GRCh37
NC_000016.8:g.163584C>A	NCBI36
NG_000006.1:g.34448C>A
NG_059186.1:g.1935C>A
NG_059271.1:g.5739C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.414C>A MANE Select	ENSP00000251595.6:p.Thr138=
ENST00000251595.10:c.414C>A	ENSP00000251595.6:p.Thr138=
ENST00000397806.1:c.318C>A	ENSP00000380908.1:p.Thr106=
ENST00000482565.1:n.550C>A
NM_000517.4:c.414C>A	NP_000508.1:p.Thr138=
NM_000517.6:c.414C>A MANE Select	NP_000508.1:p.Thr138=