Canonical Allele Identifier: CA389647735

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182530G>C , CM000676.2:g.50182530G>C	GRCh38
NC_000014.8:g.50649248G>C , CM000676.1:g.50649248G>C	GRCh37
NC_000014.7:g.49718998G>C	NCBI36
NG_051073.1:g.54164C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.791C>G MANE Select	NP_008870.2:p.Thr264Arg
ENST00000216373.10:c.791C>G MANE Select	ENSP00000216373.5:p.Thr264Arg
NM_006939.2:c.791C>G	NP_008870.2:p.Thr264Arg
NM_006939.3:c.791C>G	NP_008870.2:p.Thr264Arg
ENST00000216373.9:c.791C>G	ENSP00000216373.5:p.Thr264Arg
ENST00000543680.5:c.791C>G	ENSP00000445328.1:p.Thr264Arg
ENST00000556469.5:n.558C>G
XM_005268021.1:c.611C>G	XP_005268078.1:p.Thr204Arg
XM_011537103.1:c.752C>G	XP_011535405.1:p.Thr251Arg
XM_011537104.1:c.791C>G	XP_011535406.1:p.Thr264Arg
XR_943842.1:n.954-1257G>C
XR_943843.1:n.954-1257G>C