Canonical Allele Identifier: CA2200881049
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173678C= , CM000678.2:g.173678C= GRCh38
NC_000016.9:g.223677C= , CM000678.1:g.223677C= GRCh37
NC_000016.8:g.163677C= NCBI36
NG_000006.1:g.34541C=
NG_059186.1:g.2028C=
NG_059271.1:g.5832C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.*78C= MANE Select ENSP00000251595.6:n.*78C=
ENST00000251595.10:c.*78C= ENSP00000251595.6:n.*78C=
ENST00000397806.1:c.*78C= ENSP00000380908.1:n.*78C=
NM_000517.4:c.*78C= NP_000508.1:n.*78C=
NM_000517.6:c.*78C= MANE Select NP_000508.1:n.*78C=
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