Canonical Allele Identifier: CA2042816494
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964549T= , CM000674.2:g.65964549T= GRCh38
NC_000012.11:g.66358329T= , CM000674.1:g.66358329T= GRCh37
NC_000012.10:g.64644596T= NCBI36
NG_016296.1:g.145090T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1257T= MANE Select ENSP00000384026.2:n.*1257T=
ENST00000403681.6:c.*1257T= ENSP00000384026.2:n.*1257T=
NM_003483.4:c.*1257T= NP_003474.1:n.*1257T=
NM_003483.6:c.*1257T= MANE Select NP_003474.1:n.*1257T=