Canonical Allele Identifier: CA2042816513
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964579C= , CM000674.2:g.65964579C= GRCh38
NC_000012.11:g.66358359C= , CM000674.1:g.66358359C= GRCh37
NC_000012.10:g.64644626C= NCBI36
NG_016296.1:g.145120C=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1287C= MANE Select ENSP00000384026.2:n.*1287C=
ENST00000403681.6:c.*1287C= ENSP00000384026.2:n.*1287C=
NM_003483.4:c.*1287C= NP_003474.1:n.*1287C=
NM_003483.6:c.*1287C= MANE Select NP_003474.1:n.*1287C=