Canonical Allele Identifier: CA2042816537
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964622A= , CM000674.2:g.65964622A= GRCh38
NC_000012.11:g.66358402A= , CM000674.1:g.66358402A= GRCh37
NC_000012.10:g.64644669A= NCBI36
NG_016296.1:g.145163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1330A= MANE Select ENSP00000384026.2:n.*1330A=
ENST00000403681.6:c.*1330A= ENSP00000384026.2:n.*1330A=
NM_003483.4:c.*1330A= NP_003474.1:n.*1330A=
NM_003483.6:c.*1330A= MANE Select NP_003474.1:n.*1330A=