Canonical Allele Identifier: CA2042816535
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1159882231

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964625dup , CM000674.2:g.65964625dup GRCh38
NC_000012.11:g.66358405dup , CM000674.1:g.66358405dup GRCh37
NC_000012.10:g.64644672dup NCBI36
NG_016296.1:g.145166dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1333dup MANE Select ENSP00000384026.2:n.*1333dup
ENST00000403681.6:c.*1333dup ENSP00000384026.2:n.*1333dup
NM_003483.4:c.*1333dup NP_003474.1:n.*1333dup
NM_003483.6:c.*1333dup MANE Select NP_003474.1:n.*1333dup