Canonical Allele Identifier: CA2619690414
Gene: HMGA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964606_65964607del , CM000674.2:g.65964606_65964607del GRCh38
NC_000012.11:g.66358386_66358387del , CM000674.1:g.66358386_66358387del GRCh37
NC_000012.10:g.64644653_64644654del NCBI36
NG_016296.1:g.145147_145148del

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1314_*1315del MANE Select ENSP00000384026.2:n.*1314_*1315del
ENST00000403681.6:c.*1314_*1315del ENSP00000384026.2:n.*1314_*1315del
NM_003483.4:c.*1314_*1315del NP_003474.1:n.*1314_*1315del
NM_003483.6:c.*1314_*1315del MANE Select NP_003474.1:n.*1314_*1315del