Canonical Allele Identifier: CA2200880546
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173033C= , CM000678.2:g.173033C= GRCh38
NC_000016.9:g.223032C= , CM000678.1:g.223032C= GRCh37
NC_000016.8:g.163032C= NCBI36
NG_000006.1:g.33896C=
NG_059186.1:g.1383C=
NG_059271.1:g.5187C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.95+26C= MANE Select ENSP00000251595.6:n.95+26C=
ENST00000251595.10:c.95+26C= ENSP00000251595.6:n.95+26C=
ENST00000397806.1:c.-2+75C= ENSP00000380908.1:n.-2+75C=
ENST00000482565.1:n.140C=
ENST00000484216.1:n.64+26C=
NM_000517.4:c.95+26C= NP_000508.1:n.95+26C=
NM_000517.6:c.95+26C= MANE Select NP_000508.1:n.95+26C=
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