Canonical Allele Identifier: CA2136086434
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50182501G= , CM000676.2:g.50182501G= GRCh38
NC_000014.8:g.50649219G= , CM000676.1:g.50649219G= GRCh37
NC_000014.7:g.49718969G= NCBI36
NG_051073.1:g.54193C=

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.820C= MANE Select ENSP00000216373.5:p.His274=
ENST00000216373.9:c.820C= ENSP00000216373.5:p.His274=
ENST00000543680.5:c.820C= ENSP00000445328.1:p.His274=
ENST00000556469.5:n.587C=
NM_006939.2:c.820C= NP_008870.2:p.His274=
XM_005268021.1:c.640C= XP_005268078.1:p.His214=
XM_011537103.1:c.781C= XP_011535405.1:p.His261=
XM_011537104.1:c.820C= XP_011535406.1:p.His274=
XR_943842.1:n.954-1286G=
XR_943843.1:n.954-1286G=
NM_006939.3:c.820C= NP_008870.2:p.His274=
NM_006939.4:c.820C= MANE Select NP_008870.2:p.His274=