Canonical Allele Identifier: CA389643975
Gene: SOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1388598675

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150191A>C , CM000676.2:g.50150191A>C GRCh38
NC_000014.8:g.50616909A>C , CM000676.1:g.50616909A>C GRCh37
NC_000014.7:g.49686659A>C NCBI36
NG_051073.1:g.86503T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2201T>G MANE Select ENSP00000216373.5:p.Ile734Ser
ENST00000216373.9:c.2201T>G ENSP00000216373.5:p.Ile734Ser
ENST00000543680.5:c.2102T>G ENSP00000445328.1:p.Ile701Ser
NM_006939.2:c.2201T>G NP_008870.2:p.Ile734Ser
XM_005268021.1:c.2021T>G XP_005268078.1:p.Ile674Ser
XM_011537103.1:c.2162T>G XP_011535405.1:p.Ile721Ser
XM_011537104.1:c.2201T>G XP_011535406.1:p.Ile734Ser
NM_006939.3:c.2201T>G NP_008870.2:p.Ile734Ser
NM_006939.4:c.2201T>G MANE Select NP_008870.2:p.Ile734Ser