Canonical Allele Identifier: CA2136084728
Gene: SOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180724T= , CM000676.2:g.50180724T= GRCh38
NC_000014.8:g.50647442T= , CM000676.1:g.50647442T= GRCh37
NC_000014.7:g.49717192T= NCBI36
NG_051073.1:g.55970A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.859-42A= MANE Select ENSP00000216373.5:n.859-42A=
ENST00000216373.9:c.859-42A= ENSP00000216373.5:n.859-42A=
ENST00000543680.5:c.859-42A= ENSP00000445328.1:n.859-42A=
NM_006939.2:c.859-42A= NP_008870.2:n.859-42A=
XM_005268021.1:c.679-42A= XP_005268078.1:n.679-42A=
XM_011537103.1:c.820-42A= XP_011535405.1:n.820-42A=
XM_011537104.1:c.859-42A= XP_011535406.1:n.859-42A=
XR_943842.1:n.954-3063T=
XR_943843.1:n.954-3063T=
NM_006939.3:c.859-42A= NP_008870.2:n.859-42A=
NM_006939.4:c.859-42A= MANE Select NP_008870.2:n.859-42A=
Search 100 bp 5'
Search 100 bp 3'