Canonical Allele Identifier: CA2042817532

Gene: HMGA2

Linked Data

• dbSNP Id: rs1876894994

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65965929T>C , CM000674.2:g.65965929T>C	GRCh38
NC_000012.11:g.66359709T>C , CM000674.1:g.66359709T>C	GRCh37
NC_000012.10:g.64645976T>C	NCBI36
NG_016296.1:g.146470T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403681.7:c.*2637T>C MANE Select	ENSP00000384026.2:n.*2637T>C
ENST00000403681.6:c.*2637T>C	ENSP00000384026.2:n.*2637T>C
NM_003483.4:c.*2637T>C	NP_003474.1:n.*2637T>C
NM_003483.6:c.*2637T>C MANE Select	NP_003474.1:n.*2637T>C