Canonical Allele Identifier: CA2200880541
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173029C= , CM000678.2:g.173029C= GRCh38
NC_000016.9:g.223028C= , CM000678.1:g.223028C= GRCh37
NC_000016.8:g.163028C= NCBI36
NG_000006.1:g.33892C=
NG_059186.1:g.1379C=
NG_059271.1:g.5183C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.95+22C= MANE Select ENSP00000251595.6:n.95+22C=
ENST00000251595.10:c.95+22C= ENSP00000251595.6:n.95+22C=
ENST00000397806.1:c.-2+71C= ENSP00000380908.1:n.-2+71C=
ENST00000482565.1:n.136C=
ENST00000484216.1:n.64+22C=
NM_000517.4:c.95+22C= NP_000508.1:n.95+22C=
NM_000517.6:c.95+22C= MANE Select NP_000508.1:n.95+22C=
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