Canonical Allele Identifier: CA393993195
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs2142017740

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173006A>G , CM000678.2:g.173006A>G GRCh38
NC_000016.9:g.223005A>G , CM000678.1:g.223005A>G GRCh37
NC_000016.8:g.163005A>G NCBI36
NG_000006.1:g.33869A>G
NG_059186.1:g.1356A>G
NG_059271.1:g.5160A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.94A>G MANE Select ENSP00000251595.6:p.Arg32Gly
ENST00000251595.10:c.94A>G ENSP00000251595.6:p.Arg32Gly
ENST00000397806.1:c.-2+48A>G ENSP00000380908.1:n.-2+48A>G
ENST00000482565.1:n.113A>G
ENST00000484216.1:n.63A>G
NM_000517.4:c.94A>G NP_000508.1:p.Arg32Gly
NM_000517.6:c.94A>G MANE Select NP_000508.1:p.Arg32Gly