Canonical Allele Identifier: CA2200881052
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902068612
gnomAD v4: 16-173680-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173680T>A , CM000678.2:g.173680T>A GRCh38
NC_000016.9:g.223679T>A , CM000678.1:g.223679T>A GRCh37
NC_000016.8:g.163679T>A NCBI36
NG_000006.1:g.34543T>A
NG_059186.1:g.2030T>A
NG_059271.1:g.5834T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.*80T>A MANE Select ENSP00000251595.6:n.*80T>A
ENST00000251595.10:c.*80T>A ENSP00000251595.6:n.*80T>A
ENST00000397806.1:c.*80T>A ENSP00000380908.1:n.*80T>A
NM_000517.4:c.*80T>A NP_000508.1:n.*80T>A
NM_000517.6:c.*80T>A MANE Select NP_000508.1:n.*80T>A
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