Canonical Allele Identifier: CA2042817597

Gene: HMGA2

Linked Data

• dbSNP Id: rs1876897952

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65965997_65965998dup , CM000674.2:g.65965997_65965998dup	GRCh38
NC_000012.11:g.66359777_66359778dup , CM000674.1:g.66359777_66359778dup	GRCh37
NC_000012.10:g.64646044_64646045dup	NCBI36
NG_016296.1:g.146538_146539dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.*2705_*2706dup MANE Select	ENSP00000384026.2:n.*2705_*2706dup
ENST00000403681.6:c.*2705_*2706dup	ENSP00000384026.2:n.*2705_*2706dup
NM_003483.4:c.*2705_*2706dup	NP_003474.1:n.*2705_*2706dup
NM_003483.6:c.*2705_*2706dup MANE Select	NP_003474.1:n.*2705_*2706dup