Canonical Allele Identifier: CA7177329

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50161491C>T , CM000676.2:g.50161491C>T	GRCh38
NC_000014.8:g.50628209C>T , CM000676.1:g.50628209C>T	GRCh37
NC_000014.7:g.49697959C>T	NCBI36
NG_051073.1:g.75203G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.1187G>A MANE Select	NP_008870.2:p.Arg396His
ENST00000216373.10:c.1187G>A MANE Select	ENSP00000216373.5:p.Arg396His
NM_006939.2:c.1187G>A	NP_008870.2:p.Arg396His
NM_006939.3:c.1187G>A	NP_008870.2:p.Arg396His
ENST00000216373.9:c.1187G>A	ENSP00000216373.5:p.Arg396His
ENST00000543680.5:c.1088G>A	ENSP00000445328.1:p.Arg363His
ENST00000555794.2:c.301G>A
XM_005268021.1:c.1007G>A	XP_005268078.1:p.Arg336His
XM_011537103.1:c.1148G>A	XP_011535405.1:p.Arg383His
XM_011537104.1:c.1187G>A	XP_011535406.1:p.Arg396His