Canonical Allele Identifier: CA963008952
Gene: SOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1885705617
gnomAD v3: 14-50180706-GC-G
gnomAD v4: 14-50180706-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50180707del , CM000676.2:g.50180707del GRCh38
NC_000014.8:g.50647425del , CM000676.1:g.50647425del GRCh37
NC_000014.7:g.49717175del NCBI36
NG_051073.1:g.55987del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.859-25del MANE Select ENSP00000216373.5:n.859-25del
ENST00000216373.9:c.859-25del ENSP00000216373.5:n.859-25del
ENST00000543680.5:c.859-25del ENSP00000445328.1:n.859-25del
NM_006939.2:c.859-25del NP_008870.2:n.859-25del
XM_005268021.1:c.679-25del XP_005268078.1:n.679-25del
XM_011537103.1:c.820-25del XP_011535405.1:n.820-25del
XM_011537104.1:c.859-25del XP_011535406.1:n.859-25del
XR_943842.1:n.954-3080del
XR_943843.1:n.954-3080del
NM_006939.3:c.859-25del NP_008870.2:n.859-25del
NM_006939.4:c.859-25del MANE Select NP_008870.2:n.859-25del
Search 100 bp 5'
Search 100 bp 3'