Canonical Allele Identifier: CA2042816365
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964395C= , CM000674.2:g.65964395C= GRCh38
NC_000012.11:g.66358175C= , CM000674.1:g.66358175C= GRCh37
NC_000012.10:g.64644442C= NCBI36
NG_016296.1:g.144936C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1103C= MANE Select ENSP00000384026.2:n.*1103C=
ENST00000403681.6:c.*1103C= ENSP00000384026.2:n.*1103C=
NM_003483.4:c.*1103C= NP_003474.1:n.*1103C=
NM_003483.6:c.*1103C= MANE Select NP_003474.1:n.*1103C=
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