Canonical Allele Identifier: CA2136066030

Gene: SOS2

Linked Data

• dbSNP Id: rs1884709881

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153003dup , CM000676.2:g.50153003dup	GRCh38
NC_000014.8:g.50619721dup , CM000676.1:g.50619721dup	GRCh37
NC_000014.7:g.49689471dup	NCBI36
NG_051073.1:g.83693dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+69dup MANE Select	ENSP00000216373.5:n.2161+69dup
ENST00000216373.9:c.2161+69dup	ENSP00000216373.5:n.2161+69dup
ENST00000543680.5:c.2062+69dup	ENSP00000445328.1:n.2062+69dup
NM_006939.2:c.2161+69dup	NP_008870.2:n.2161+69dup
XM_005268021.1:c.1981+69dup	XP_005268078.1:n.1981+69dup
XM_011537103.1:c.2122+69dup	XP_011535405.1:n.2122+69dup
XM_011537104.1:c.2161+69dup	XP_011535406.1:n.2161+69dup
NM_006939.3:c.2161+69dup	NP_008870.2:n.2161+69dup
NM_006939.4:c.2161+69dup MANE Select	NP_008870.2:n.2161+69dup