Canonical Allele Identifier: CA2200880534

Gene: HBA2

Linked Data

• dbSNP Id: rs1902040027

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173021C>G , CM000678.2:g.173021C>G	GRCh38
NC_000016.9:g.223020C>G , CM000678.1:g.223020C>G	GRCh37
NC_000016.8:g.163020C>G	NCBI36
NG_000006.1:g.33884C>G
NG_059186.1:g.1371C>G
NG_059271.1:g.5175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.95+14C>G MANE Select	ENSP00000251595.6:n.95+14C>G
ENST00000251595.10:c.95+14C>G	ENSP00000251595.6:n.95+14C>G
ENST00000397806.1:c.-2+63C>G	ENSP00000380908.1:n.-2+63C>G
ENST00000482565.1:n.128C>G
ENST00000484216.1:n.64+14C>G
NM_000517.4:c.95+14C>G	NP_000508.1:n.95+14C>G
NM_000517.6:c.95+14C>G MANE Select	NP_000508.1:n.95+14C>G