Canonical Allele Identifier: CA2619690412
Gene: HMGA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964597T>C , CM000674.2:g.65964597T>C GRCh38
NC_000012.11:g.66358377T>C , CM000674.1:g.66358377T>C GRCh37
NC_000012.10:g.64644644T>C NCBI36
NG_016296.1:g.145138T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1305T>C MANE Select ENSP00000384026.2:n.*1305T>C
ENST00000403681.6:c.*1305T>C ENSP00000384026.2:n.*1305T>C
NM_003483.4:c.*1305T>C NP_003474.1:n.*1305T>C
NM_003483.6:c.*1305T>C MANE Select NP_003474.1:n.*1305T>C