Canonical Allele Identifier: CA655098239
Gene: HMGA2 HGNC NCBI

Linked Data

COSMIC: COSN21857329 COSN24237839
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965875_65965876insC , CM000674.2:g.65965875_65965876insC GRCh38
NC_000012.11:g.66359655_66359656insC , CM000674.1:g.66359655_66359656insC GRCh37
NC_000012.10:g.64645922_64645923insC NCBI36
NG_016296.1:g.146416_146417insC

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2583_*2584insC MANE Select ENSP00000384026.2:n.*2583_*2584insC
ENST00000403681.6:c.*2583_*2584insC ENSP00000384026.2:n.*2583_*2584insC
NM_003483.4:c.*2583_*2584insC NP_003474.1:n.*2583_*2584insC
NM_003483.6:c.*2583_*2584insC MANE Select NP_003474.1:n.*2583_*2584insC
Search 100 bp 5'
Search 100 bp 3'