Canonical Allele Identifier: CA7177129
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785778
dbSNP Id: rs750920712

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50153137A>G , CM000676.2:g.50153137A>G GRCh38
NC_000014.8:g.50619855A>G , CM000676.1:g.50619855A>G GRCh37
NC_000014.7:g.49689605A>G NCBI36
NG_051073.1:g.83557T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2094T>C MANE Select ENSP00000216373.5:p.His698=
ENST00000216373.9:c.2094T>C ENSP00000216373.5:p.His698=
ENST00000543680.5:c.1995T>C ENSP00000445328.1:p.His665=
NM_006939.2:c.2094T>C NP_008870.2:p.His698=
XM_005268021.1:c.1914T>C XP_005268078.1:p.His638=
XM_011537103.1:c.2055T>C XP_011535405.1:p.His685=
XM_011537104.1:c.2094T>C XP_011535406.1:p.His698=
NM_006939.3:c.2094T>C NP_008870.2:p.His698=
NM_006939.4:c.2094T>C MANE Select NP_008870.2:p.His698=