Canonical Allele Identifier: CA2136066077
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50153137A= , CM000676.2:g.50153137A= GRCh38
NC_000014.8:g.50619855A= , CM000676.1:g.50619855A= GRCh37
NC_000014.7:g.49689605A= NCBI36
NG_051073.1:g.83557T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2094T= MANE Select ENSP00000216373.5:p.His698=
ENST00000216373.9:c.2094T= ENSP00000216373.5:p.His698=
ENST00000543680.5:c.1995T= ENSP00000445328.1:p.His665=
NM_006939.2:c.2094T= NP_008870.2:p.His698=
XM_005268021.1:c.1914T= XP_005268078.1:p.His638=
XM_011537103.1:c.2055T= XP_011535405.1:p.His685=
XM_011537104.1:c.2094T= XP_011535406.1:p.His698=
NM_006939.3:c.2094T= NP_008870.2:p.His698=
NM_006939.4:c.2094T= MANE Select NP_008870.2:p.His698=