Canonical Allele Identifier: CA276415497
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs41514946

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173573C>G , CM000678.2:g.173573C>G GRCh38
NC_000016.9:g.223572C>G , CM000678.1:g.223572C>G GRCh37
NC_000016.8:g.163572C>G NCBI36
NG_000006.1:g.34436C>G
NG_059186.1:g.1923C>G
NG_059271.1:g.5727C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.402C>G MANE Select ENSP00000251595.6:p.Ser134Arg
ENST00000251595.10:c.402C>G ENSP00000251595.6:p.Ser134Arg
ENST00000397806.1:c.306C>G ENSP00000380908.1:p.Ser102Arg
ENST00000482565.1:n.538C>G
NM_000517.4:c.402C>G NP_000508.1:p.Ser134Arg
NM_000517.6:c.402C>G MANE Select NP_000508.1:p.Ser134Arg