Canonical Allele Identifier: CA1139663472

Gene: SOS2

Linked Data

• ClinVar Variation Id: 928959
• ClinVar RCV Id: RCV001193654
• dbSNP Id: rs1884615891

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150161_50150257dup , CM000676.2:g.50150161_50150257dup	GRCh38
NC_000014.8:g.50616879_50616975dup , CM000676.1:g.50616879_50616975dup	GRCh37
NC_000014.7:g.49686629_49686725dup	NCBI36
NG_051073.1:g.86437_86533dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2162-27_2231dup
ENST00000216373.9:c.2162-27_2231dup
ENST00000543680.5:c.2063-27_2132dup
NM_006939.2:c.2162-27_2231dup
XM_005268021.1:c.1982-27_2051dup
XM_011537103.1:c.2123-27_2192dup
XM_011537104.1:c.2162-27_2231dup
NM_006939.3:c.2162-27_2231dup
NM_006939.4:c.2162-27_2231dup