Canonical Allele Identifier: CA389644082

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50619788C>G (hg19) ; chr14:g.50153070C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153070C>G , CM000676.2:g.50153070C>G	GRCh38
NC_000014.8:g.50619788C>G , CM000676.1:g.50619788C>G	GRCh37
NC_000014.7:g.49689538C>G	NCBI36
NG_051073.1:g.83624G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2161G>C MANE Select	ENSP00000216373.5:p.Gly721Arg
ENST00000216373.9:c.2161G>C	ENSP00000216373.5:p.Gly721Arg
ENST00000543680.5:c.2062G>C	ENSP00000445328.1:p.Gly688Arg
NM_006939.2:c.2161G>C	NP_008870.2:p.Gly721Arg
XM_005268021.1:c.1981G>C	XP_005268078.1:p.Gly661Arg
XM_011537103.1:c.2122G>C	XP_011535405.1:p.Gly708Arg
XM_011537104.1:c.2161G>C	XP_011535406.1:p.Gly721Arg
NM_006939.3:c.2161G>C	NP_008870.2:p.Gly721Arg
NM_006939.4:c.2161G>C MANE Select	NP_008870.2:p.Gly721Arg