Canonical Allele Identifier: CA276415491
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs33960790

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173571A>C , CM000678.2:g.173571A>C GRCh38
NC_000016.9:g.223570A>C , CM000678.1:g.223570A>C GRCh37
NC_000016.8:g.163570A>C NCBI36
NG_000006.1:g.34434A>C
NG_059186.1:g.1921A>C
NG_059271.1:g.5725A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.400A>C MANE Select ENSP00000251595.6:p.Ser134Arg
ENST00000251595.10:c.400A>C ENSP00000251595.6:p.Ser134Arg
ENST00000397806.1:c.304A>C ENSP00000380908.1:p.Ser102Arg
ENST00000482565.1:n.536A>C
NM_000517.4:c.400A>C NP_000508.1:p.Ser134Arg
NM_000517.6:c.400A>C MANE Select NP_000508.1:p.Ser134Arg