Canonical Allele Identifier: CA2548433265

Gene: HMGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65965897T>G , CM000674.2:g.65965897T>G	GRCh38
NC_000012.11:g.66359677T>G , CM000674.1:g.66359677T>G	GRCh37
NC_000012.10:g.64645944T>G	NCBI36
NG_016296.1:g.146438T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403681.7:c.*2605T>G MANE Select	ENSP00000384026.2:n.*2605T>G
ENST00000403681.6:c.*2605T>G	ENSP00000384026.2:n.*2605T>G
NM_003483.4:c.*2605T>G	NP_003474.1:n.*2605T>G
NM_003483.6:c.*2605T>G MANE Select	NP_003474.1:n.*2605T>G