Canonical Allele Identifier: CA2042816496
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1876853235
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964549_65964550insCAGATGTATTAAGTC , CM000674.2:g.65964549_65964550insCAGATGTATTAAGTC GRCh38
NC_000012.11:g.66358329_66358330insCAGATGTATTAAGTC , CM000674.1:g.66358329_66358330insCAGATGTATTAAGTC GRCh37
NC_000012.10:g.64644596_64644597insCAGATGTATTAAGTC NCBI36
NG_016296.1:g.145090_145091insCAGATGTATTAAGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1257_*1258insCAGATGTATTAAGTC MANE Select ENSP00000384026.2:n.*1257_*1258insCAGATGTATTAAGTC
ENST00000403681.6:c.*1257_*1258insCAGATGTATTAAGTC ENSP00000384026.2:n.*1257_*1258insCAGATGTATTAAGTC
NM_003483.4:c.*1257_*1258insCAGATGTATTAAGTC NP_003474.1:n.*1257_*1258insCAGATGTATTAAGTC
NM_003483.6:c.*1257_*1258insCAGATGTATTAAGTC MANE Select NP_003474.1:n.*1257_*1258insCAGATGTATTAAGTC
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