Canonical Allele Identifier: CA2796347594
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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