Canonical Allele Identifier: CA7176682
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 475758
dbSNP Id: rs140995728

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50118391G>A , CM000676.2:g.50118391G>A GRCh38
NC_000014.8:g.50585109G>A , CM000676.1:g.50585109G>A GRCh37
NC_000014.7:g.49654859G>A NCBI36
NG_051073.1:g.118303C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.3952C>T MANE Select ENSP00000216373.5:p.Pro1318Ser
ENST00000216373.9:c.3952C>T ENSP00000216373.5:p.Pro1318Ser
ENST00000543680.5:c.3853C>T ENSP00000445328.1:p.Pro1285Ser
NM_006939.2:c.3952C>T NP_008870.2:p.Pro1318Ser
XM_005268021.1:c.3772C>T XP_005268078.1:p.Pro1258Ser
XM_011537103.1:c.3913C>T XP_011535405.1:p.Pro1305Ser
NM_006939.3:c.3952C>T NP_008870.2:p.Pro1318Ser
NM_006939.4:c.3952C>T MANE Select NP_008870.2:p.Pro1318Ser