Canonical Allele Identifier: CA393993397
Gene: HBA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173181A>C , CM000678.2:g.173181A>C GRCh38
NC_000016.9:g.223180A>C , CM000678.1:g.223180A>C GRCh37
NC_000016.8:g.163180A>C NCBI36
NG_000006.1:g.34044A>C
NG_059186.1:g.1531A>C
NG_059271.1:g.5335A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.152A>C MANE Select ENSP00000251595.6:p.His51Pro
ENST00000251595.10:c.152A>C ENSP00000251595.6:p.His51Pro
ENST00000397806.1:c.56A>C ENSP00000380908.1:p.His19Pro
ENST00000482565.1:n.288A>C
ENST00000484216.1:n.121A>C
NM_000517.4:c.152A>C NP_000508.1:p.His51Pro
NM_000517.6:c.152A>C MANE Select NP_000508.1:p.His51Pro