Canonical Allele Identifier: CA276414780
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864850

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173223A>G , CM000678.2:g.173223A>G GRCh38
NC_000016.9:g.223222A>G , CM000678.1:g.223222A>G GRCh37
NC_000016.8:g.163222A>G NCBI36
NG_000006.1:g.34086A>G
NG_059186.1:g.1573A>G
NG_059271.1:g.5377A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.194A>G MANE Select ENSP00000251595.6:p.Asp65Gly
ENST00000251595.10:c.194A>G ENSP00000251595.6:p.Asp65Gly
ENST00000397806.1:c.98A>G ENSP00000380908.1:p.Asp33Gly
ENST00000482565.1:n.330A>G
ENST00000484216.1:n.163A>G
NM_000517.4:c.194A>G NP_000508.1:p.Asp65Gly
NM_000517.6:c.194A>G MANE Select NP_000508.1:p.Asp65Gly