Canonical Allele Identifier: CA389646948
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180597C>G , CM000676.2:g.50180597C>G GRCh38
NC_000014.8:g.50647315C>G , CM000676.1:g.50647315C>G GRCh37
NC_000014.7:g.49717065C>G NCBI36
NG_051073.1:g.56097G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.944G>C MANE Select ENSP00000216373.5:p.Arg315Thr
ENST00000216373.9:c.944G>C ENSP00000216373.5:p.Arg315Thr
ENST00000543680.5:c.944G>C ENSP00000445328.1:p.Arg315Thr
ENST00000555794.2:c.58G>C
NM_006939.2:c.944G>C NP_008870.2:p.Arg315Thr
XM_005268021.1:c.764G>C XP_005268078.1:p.Arg255Thr
XM_011537103.1:c.905G>C XP_011535405.1:p.Arg302Thr
XM_011537104.1:c.944G>C XP_011535406.1:p.Arg315Thr
XR_943842.1:n.954-3190C>G
XR_943843.1:n.954-3190C>G
NM_006939.3:c.944G>C NP_008870.2:p.Arg315Thr
NM_006939.4:c.944G>C MANE Select NP_008870.2:p.Arg315Thr