Canonical Allele Identifier: CA2042816540
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964624A= , CM000674.2:g.65964624A= GRCh38
NC_000012.11:g.66358404A= , CM000674.1:g.66358404A= GRCh37
NC_000012.10:g.64644671A= NCBI36
NG_016296.1:g.145165A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1332A= MANE Select ENSP00000384026.2:n.*1332A=
ENST00000403681.6:c.*1332A= ENSP00000384026.2:n.*1332A=
NM_003483.4:c.*1332A= NP_003474.1:n.*1332A=
NM_003483.6:c.*1332A= MANE Select NP_003474.1:n.*1332A=