Canonical Allele Identifier: CA7177471

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50188502G>T , CM000676.2:g.50188502G>T	GRCh38
NC_000014.8:g.50655220G>T , CM000676.1:g.50655220G>T	GRCh37
NC_000014.7:g.49724970G>T	NCBI36
NG_051073.1:g.48192C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006939.4:c.709C>A MANE Select	NP_008870.2:p.Pro237Thr
ENST00000216373.10:c.709C>A MANE Select	ENSP00000216373.5:p.Pro237Thr
NM_006939.2:c.709C>A	NP_008870.2:p.Pro237Thr
NM_006939.3:c.709C>A	NP_008870.2:p.Pro237Thr
ENST00000216373.9:c.709C>A	ENSP00000216373.5:p.Pro237Thr
ENST00000543680.5:c.709C>A	ENSP00000445328.1:p.Pro237Thr
ENST00000556469.5:n.482-5896C>A
XM_005268021.1:c.529C>A	XP_005268078.1:p.Pro177Thr
XM_011537103.1:c.670C>A	XP_011535405.1:p.Pro224Thr
XM_011537104.1:c.709C>A	XP_011535406.1:p.Pro237Thr
XR_943842.1:n.1039+4630G>T
XR_943843.1:n.1039+4630G>T