Canonical Allele Identifier: CA691031984

Gene: HMGA2

Linked Data

• dbSNP Id: rs1171764425
• MyVariant Identifiers: chr12:g.66224475G>C (hg19) ; chr12:g.65830695G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65830695G>C , CM000674.2:g.65830695G>C	GRCh38
NC_000012.11:g.66224475G>C , CM000674.1:g.66224475G>C	GRCh37
NC_000012.10:g.64510742G>C	NCBI36
NG_016296.1:g.11236G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403681.7:c.198+2608G>C MANE Select	ENSP00000384026.2:n.198+2608G>C
ENST00000354636.7:c.198+2608G>C	ENSP00000346658.3:n.198+2608G>C
ENST00000393577.7:c.198+2608G>C	ENSP00000377205.3:n.198+2608G>C
ENST00000393578.7:c.198+2608G>C	ENSP00000377206.3:n.198+2608G>C
ENST00000403681.6:c.198+2608G>C	ENSP00000384026.2:n.198+2608G>C
ENST00000425208.6:c.198+2608G>C	ENSP00000407306.2:n.198+2608G>C
ENST00000536545.5:c.198+2608G>C	ENSP00000437621.1:n.198+2608G>C
ENST00000537275.5:c.198+2608G>C	ENSP00000437747.1:n.198+2608G>C
ENST00000537429.5:c.198+2608G>C	ENSP00000443372.1:n.198+2608G>C
ENST00000539662.1:c.87+2608G>C	ENSP00000440919.1:n.87+2608G>C
ENST00000541363.5:c.198+2608G>C	ENSP00000439317.1:n.198+2608G>C
NM_001300918.1:c.198+2608G>C	NP_001287847.1:n.198+2608G>C
NM_001300919.1:c.198+2608G>C	NP_001287848.1:n.198+2608G>C
NM_003483.4:c.198+2608G>C	NP_003474.1:n.198+2608G>C
NM_003484.1:c.198+2608G>C	NP_003475.1:n.198+2608G>C
NM_001330190.1:c.198+2608G>C	NP_001317119.1:n.198+2608G>C
NM_003483.6:c.198+2608G>C MANE Select	NP_003474.1:n.198+2608G>C