Canonical Allele Identifier: CA260719034

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50138349C>T , CM000676.2:g.50138349C>T	GRCh38
NC_000014.8:g.50605067C>T , CM000676.1:g.50605067C>T	GRCh37
NC_000014.7:g.49674817C>T	NCBI36
NG_051073.1:g.98345G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.2958+263G>A MANE Select	NP_008870.2:n.2958+263G>A
ENST00000216373.10:c.2958+263G>A MANE Select	ENSP00000216373.5:n.2958+263G>A
NM_006939.2:c.2958+263G>A	NP_008870.2:n.2958+263G>A
NM_006939.3:c.2958+263G>A	NP_008870.2:n.2958+263G>A
ENST00000216373.9:c.2958+263G>A	ENSP00000216373.5:n.2958+263G>A
ENST00000543680.5:c.2859+263G>A	ENSP00000445328.1:n.2859+263G>A
XM_005268021.1:c.2778+263G>A	XP_005268078.1:n.2778+263G>A
XM_011537103.1:c.2919+263G>A	XP_011535405.1:n.2919+263G>A
XM_011537104.1:c.2785+1593G>A	XP_011535406.1:n.2785+1593G>A