Canonical Allele Identifier: CA486175113

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50619798T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153080T>G , CM000676.2:g.50153080T>G	GRCh38
NC_000014.8:g.50619798T>G , CM000676.1:g.50619798T>G	GRCh37
NC_000014.7:g.49689548T>G	NCBI36
NG_051073.1:g.83614A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2151A>C MANE Select	ENSP00000216373.5:p.Ser717=
ENST00000216373.9:c.2151A>C	ENSP00000216373.5:p.Ser717=
ENST00000543680.5:c.2052A>C	ENSP00000445328.1:p.Ser684=
NM_006939.2:c.2151A>C	NP_008870.2:p.Ser717=
XM_005268021.1:c.1971A>C	XP_005268078.1:p.Ser657=
XM_011537103.1:c.2112A>C	XP_011535405.1:p.Ser704=
XM_011537104.1:c.2151A>C	XP_011535406.1:p.Ser717=
NM_006939.3:c.2151A>C	NP_008870.2:p.Ser717=
NM_006939.4:c.2151A>C MANE Select	NP_008870.2:p.Ser717=