Canonical Allele Identifier: CA963007686
Gene: SOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1421879437
gnomAD v3: 14-50150260-CTT-C
gnomAD v4: 14-50150260-CTT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150263_50150264del , CM000676.2:g.50150263_50150264del GRCh38
NC_000014.8:g.50616981_50616982del , CM000676.1:g.50616981_50616982del GRCh37
NC_000014.7:g.49686731_49686732del NCBI36
NG_051073.1:g.86432_86433del

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2162-32_2162-31del MANE Select ENSP00000216373.5:n.2162-32_2162-31del
ENST00000216373.9:c.2162-32_2162-31del ENSP00000216373.5:n.2162-32_2162-31del
ENST00000543680.5:c.2063-32_2063-31del ENSP00000445328.1:n.2063-32_2063-31del
NM_006939.2:c.2162-32_2162-31del NP_008870.2:n.2162-32_2162-31del
XM_005268021.1:c.1982-32_1982-31del XP_005268078.1:n.1982-32_1982-31del
XM_011537103.1:c.2123-32_2123-31del XP_011535405.1:n.2123-32_2123-31del
XM_011537104.1:c.2162-32_2162-31del XP_011535406.1:n.2162-32_2162-31del
NM_006939.3:c.2162-32_2162-31del NP_008870.2:n.2162-32_2162-31del
NM_006939.4:c.2162-32_2162-31del MANE Select NP_008870.2:n.2162-32_2162-31del
Search 100 bp 5'
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