Canonical Allele Identifier: CA2575852769

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173111G>A , CM000678.2:g.173111G>A	GRCh38
NC_000016.9:g.223110G>A , CM000678.1:g.223110G>A	GRCh37
NC_000016.8:g.163110G>A	NCBI36
NG_000006.1:g.33974G>A
NG_059186.1:g.1461G>A
NG_059271.1:g.5265G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.96-14G>A MANE Select	ENSP00000251595.6:n.96-14G>A
ENST00000251595.10:c.96-14G>A	ENSP00000251595.6:n.96-14G>A
ENST00000397806.1:c.-1-14G>A	ENSP00000380908.1:n.-1-14G>A
ENST00000482565.1:n.218G>A
ENST00000484216.1:n.65-14G>A
NM_000517.4:c.96-14G>A	NP_000508.1:n.96-14G>A
NM_000517.6:c.96-14G>A MANE Select	NP_000508.1:n.96-14G>A