Canonical Allele Identifier: CA2042816512
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964577G= , CM000674.2:g.65964577G= GRCh38
NC_000012.11:g.66358357G= , CM000674.1:g.66358357G= GRCh37
NC_000012.10:g.64644624G= NCBI36
NG_016296.1:g.145118G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1285G= MANE Select ENSP00000384026.2:n.*1285G=
ENST00000403681.6:c.*1285G= ENSP00000384026.2:n.*1285G=
NM_003483.4:c.*1285G= NP_003474.1:n.*1285G=
NM_003483.6:c.*1285G= MANE Select NP_003474.1:n.*1285G=