Canonical Allele Identifier: CA2729651141

Gene: SOS2

Linked Data

• dbSNP Id: rs2139702518

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180704A>C , CM000676.2:g.50180704A>C	GRCh38
NC_000014.8:g.50647422A>C , CM000676.1:g.50647422A>C	GRCh37
NC_000014.7:g.49717172A>C	NCBI36
NG_051073.1:g.55990T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-22T>G MANE Select	ENSP00000216373.5:n.859-22T>G
ENST00000216373.9:c.859-22T>G	ENSP00000216373.5:n.859-22T>G
ENST00000543680.5:c.859-22T>G	ENSP00000445328.1:n.859-22T>G
NM_006939.2:c.859-22T>G	NP_008870.2:n.859-22T>G
XM_005268021.1:c.679-22T>G	XP_005268078.1:n.679-22T>G
XM_011537103.1:c.820-22T>G	XP_011535405.1:n.820-22T>G
XM_011537104.1:c.859-22T>G	XP_011535406.1:n.859-22T>G
XR_943842.1:n.954-3083A>C
XR_943843.1:n.954-3083A>C
NM_006939.3:c.859-22T>G	NP_008870.2:n.859-22T>G
NM_006939.4:c.859-22T>G MANE Select	NP_008870.2:n.859-22T>G