Canonical Allele Identifier: CA2136086437
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50182505A= , CM000676.2:g.50182505A= GRCh38
NC_000014.8:g.50649223A= , CM000676.1:g.50649223A= GRCh37
NC_000014.7:g.49718973A= NCBI36
NG_051073.1:g.54189T=

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.816T= MANE Select ENSP00000216373.5:p.Ser272=
ENST00000216373.9:c.816T= ENSP00000216373.5:p.Ser272=
ENST00000543680.5:c.816T= ENSP00000445328.1:p.Ser272=
ENST00000556469.5:n.583T=
NM_006939.2:c.816T= NP_008870.2:p.Ser272=
XM_005268021.1:c.636T= XP_005268078.1:p.Ser212=
XM_011537103.1:c.777T= XP_011535405.1:p.Ser259=
XM_011537104.1:c.816T= XP_011535406.1:p.Ser272=
XR_943842.1:n.954-1282A=
XR_943843.1:n.954-1282A=
NM_006939.3:c.816T= NP_008870.2:p.Ser272=
NM_006939.4:c.816T= MANE Select NP_008870.2:p.Ser272=