Canonical Allele Identifier: CA238996350
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs746238231
MyVariant Identifiers: chr12:g.66358262G>A (hg19) chr12:g.65964482G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964482G>A , CM000674.2:g.65964482G>A GRCh38
NC_000012.11:g.66358262G>A , CM000674.1:g.66358262G>A GRCh37
NC_000012.10:g.64644529G>A NCBI36
NG_016296.1:g.145023G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1190G>A MANE Select ENSP00000384026.2:n.*1190G>A
ENST00000403681.6:c.*1190G>A ENSP00000384026.2:n.*1190G>A
NM_003483.4:c.*1190G>A NP_003474.1:n.*1190G>A
NM_003483.6:c.*1190G>A MANE Select NP_003474.1:n.*1190G>A
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