Canonical Allele Identifier: CA389640407
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130536C>G , CM000676.2:g.50130536C>G GRCh38
NC_000014.8:g.50597254C>G , CM000676.1:g.50597254C>G GRCh37
NC_000014.7:g.49667004C>G NCBI36
NG_051073.1:g.106158G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3302G>C MANE Select ENSP00000216373.5:p.Ser1101Thr
ENST00000216373.9:c.3302G>C ENSP00000216373.5:p.Ser1101Thr
ENST00000543680.5:c.3203G>C ENSP00000445328.1:p.Ser1068Thr
NM_006939.2:c.3302G>C NP_008870.2:p.Ser1101Thr
XM_005268021.1:c.3122G>C XP_005268078.1:p.Ser1041Thr
XM_011537103.1:c.3263G>C XP_011535405.1:p.Ser1088Thr
NM_006939.3:c.3302G>C NP_008870.2:p.Ser1101Thr
NM_006939.4:c.3302G>C MANE Select NP_008870.2:p.Ser1101Thr