Canonical Allele Identifier: CA2200880119

Gene: HBA2

Linked Data

• dbSNP Id: rs1596569265
• gnomAD v4: 16-172848-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172848A>G , CM000678.2:g.172848A>G	GRCh38
NC_000016.9:g.222847A>G , CM000678.1:g.222847A>G	GRCh37
NC_000016.8:g.162847A>G	NCBI36
NG_000006.1:g.33711A>G
NG_059186.1:g.1198A>G
NG_059271.1:g.5002A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.10:c.-65A>G	ENSP00000251595.6:n.-65A>G
NM_000517.4:c.-65A>G	NP_000508.1:n.-65A>G