Canonical Allele Identifier: CA276415526
Gene: HBA2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs63750801

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173586T>C , CM000678.2:g.173586T>C GRCh38
NC_000016.9:g.223585T>C , CM000678.1:g.223585T>C GRCh37
NC_000016.8:g.163585T>C NCBI36
NG_000006.1:g.34449T>C
NG_059186.1:g.1936T>C
NG_059271.1:g.5740T>C

Transcript Alleles

HGVS Amino-acid change
NM_000517.4:c.415T>C VV NP_000508.1:p.Ser139Pro
NM_000517.6:c.415T>C VV NP_000508.1:p.Ser139Pro
ENST00000251595.10:c.415T>C ENSP00000251595.6:p.Ser139Pro
ENST00000397806.1:c.319T>C ENSP00000380908.1:p.Ser107Pro
ENST00000482565.1:n.551T>C