Canonical Allele Identifier: CA492994598

Gene: HBA2

Linked Data

• MyVariant Identifiers: chr16:g.223190C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173191C>A , CM000678.2:g.173191C>A	GRCh38
NC_000016.9:g.223190C>A , CM000678.1:g.223190C>A	GRCh37
NC_000016.8:g.163190C>A	NCBI36
NG_000006.1:g.34054C>A
NG_059186.1:g.1541C>A
NG_059271.1:g.5345C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.162C>A MANE Select	ENSP00000251595.6:p.Ala54=
ENST00000251595.10:c.162C>A	ENSP00000251595.6:p.Ala54=
ENST00000397806.1:c.66C>A	ENSP00000380908.1:p.Ala22=
ENST00000482565.1:n.298C>A
ENST00000484216.1:n.131C>A
NM_000517.4:c.162C>A	NP_000508.1:p.Ala54=
NM_000517.6:c.162C>A MANE Select	NP_000508.1:p.Ala54=