Canonical Allele Identifier: CA2200881002
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173621T= , CM000678.2:g.173621T= GRCh38
NC_000016.9:g.223620T= , CM000678.1:g.223620T= GRCh37
NC_000016.8:g.163620T= NCBI36
NG_000006.1:g.34484T=
NG_059186.1:g.1971T=
NG_059271.1:g.5775T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.*21T= MANE Select ENSP00000251595.6:n.*21T=
ENST00000251595.10:c.*21T= ENSP00000251595.6:n.*21T=
ENST00000397806.1:c.*21T= ENSP00000380908.1:n.*21T=
ENST00000482565.1:n.586T=
NM_000517.4:c.*21T= NP_000508.1:n.*21T=
NM_000517.6:c.*21T= MANE Select NP_000508.1:n.*21T=
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