Canonical Allele Identifier: CA389647034
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2887770
ClinVar RCV Id: RCV003756209
dbSNP Id: rs1566840605
gnomAD v3: 14-50180634-G-A
gnomAD v4: 14-50180634-G-A
COSMIC: COSM6285341 COSM6285342
MyVariant Identifiers: chr14:g.50647352G>A (hg19) chr14:g.50180634G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180634G>A , CM000676.2:g.50180634G>A GRCh38
NC_000014.8:g.50647352G>A , CM000676.1:g.50647352G>A GRCh37
NC_000014.7:g.49717102G>A NCBI36
NG_051073.1:g.56060C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.907C>T MANE Select ENSP00000216373.5:p.Pro303Ser
ENST00000216373.9:c.907C>T ENSP00000216373.5:p.Pro303Ser
ENST00000543680.5:c.907C>T ENSP00000445328.1:p.Pro303Ser
ENST00000555794.2:c.21C>T
NM_006939.2:c.907C>T NP_008870.2:p.Pro303Ser
XM_005268021.1:c.727C>T XP_005268078.1:p.Pro243Ser
XM_011537103.1:c.868C>T XP_011535405.1:p.Pro290Ser
XM_011537104.1:c.907C>T XP_011535406.1:p.Pro303Ser
XR_943842.1:n.954-3153G>A
XR_943843.1:n.954-3153G>A
NM_006939.3:c.907C>T NP_008870.2:p.Pro303Ser
NM_006939.4:c.907C>T MANE Select NP_008870.2:p.Pro303Ser
Search 100 bp 5'
Search 100 bp 3'