Canonical Allele Identifier: CA276415377
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864887
gnomAD v4: 16-173514-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173514C>G , CM000678.2:g.173514C>G GRCh38
NC_000016.9:g.223513C>G , CM000678.1:g.223513C>G GRCh37
NC_000016.8:g.163513C>G NCBI36
NG_000006.1:g.34377C>G
NG_059186.1:g.1864C>G
NG_059271.1:g.5668C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.343C>G MANE Select ENSP00000251595.6:p.Pro115Ala
ENST00000251595.10:c.343C>G ENSP00000251595.6:p.Pro115Ala
ENST00000397806.1:c.247C>G ENSP00000380908.1:p.Pro83Ala
ENST00000482565.1:n.479C>G
NM_000517.4:c.343C>G NP_000508.1:p.Pro115Ala
NM_000517.6:c.343C>G MANE Select NP_000508.1:p.Pro115Ala