Canonical Allele Identifier: CA2630738160
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173696-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173696T>A , CM000678.2:g.173696T>A GRCh38
NC_000016.9:g.223695T>A , CM000678.1:g.223695T>A GRCh37
NC_000016.8:g.163695T>A NCBI36
NG_000006.1:g.34559T>A
NG_059186.1:g.2046T>A
NG_059271.1:g.5850T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.*96T>A MANE Select ENSP00000251595.6:n.*96T>A
ENST00000251595.10:c.*96T>A ENSP00000251595.6:n.*96T>A
ENST00000397806.1:c.*96T>A ENSP00000380908.1:n.*96T>A
NM_000517.4:c.*96T>A NP_000508.1:n.*96T>A
NM_000517.6:c.*96T>A MANE Select NP_000508.1:n.*96T>A
Search 100 bp 5'
Search 100 bp 3'