Canonical Allele Identifier: CA276414993
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864867

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173292A>G , CM000678.2:g.173292A>G GRCh38
NC_000016.9:g.223291A>G , CM000678.1:g.223291A>G GRCh37
NC_000016.8:g.163291A>G NCBI36
NG_000006.1:g.34155A>G
NG_059186.1:g.1642A>G
NG_059271.1:g.5446A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.263A>G MANE Select ENSP00000251595.6:p.His88Arg
ENST00000251595.10:c.263A>G ENSP00000251595.6:p.His88Arg
ENST00000397806.1:c.167A>G ENSP00000380908.1:p.His56Arg
ENST00000482565.1:n.399A>G
ENST00000484216.1:n.232A>G
NM_000517.4:c.263A>G NP_000508.1:p.His88Arg
NM_000517.6:c.263A>G MANE Select NP_000508.1:p.His88Arg