Canonical Allele Identifier: CA389644237

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50619856T>C (hg19) ; chr14:g.50153138T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153138T>C , CM000676.2:g.50153138T>C	GRCh38
NC_000014.8:g.50619856T>C , CM000676.1:g.50619856T>C	GRCh37
NC_000014.7:g.49689606T>C	NCBI36
NG_051073.1:g.83556A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2093A>G MANE Select	ENSP00000216373.5:p.His698Arg
ENST00000216373.9:c.2093A>G	ENSP00000216373.5:p.His698Arg
ENST00000543680.5:c.1994A>G	ENSP00000445328.1:p.His665Arg
NM_006939.2:c.2093A>G	NP_008870.2:p.His698Arg
XM_005268021.1:c.1913A>G	XP_005268078.1:p.His638Arg
XM_011537103.1:c.2054A>G	XP_011535405.1:p.His685Arg
XM_011537104.1:c.2093A>G	XP_011535406.1:p.His698Arg
NM_006939.3:c.2093A>G	NP_008870.2:p.His698Arg
NM_006939.4:c.2093A>G MANE Select	NP_008870.2:p.His698Arg