Canonical Allele Identifier: CA963009078

Gene: SOS2

Linked Data

• dbSNP Id: rs1885710451
• gnomAD v3: 14-50180861-GA-G
• gnomAD v4: 14-50180861-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180865del , CM000676.2:g.50180865del	GRCh38
NC_000014.8:g.50647583del , CM000676.1:g.50647583del	GRCh37
NC_000014.7:g.49717333del	NCBI36
NG_051073.1:g.55832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-180del MANE Select	ENSP00000216373.5:n.859-180del
ENST00000216373.9:c.859-180del	ENSP00000216373.5:n.859-180del
ENST00000543680.5:c.859-180del	ENSP00000445328.1:n.859-180del
NM_006939.2:c.859-180del	NP_008870.2:n.859-180del
XM_005268021.1:c.679-180del	XP_005268078.1:n.679-180del
XM_011537103.1:c.820-180del	XP_011535405.1:n.820-180del
XM_011537104.1:c.859-180del	XP_011535406.1:n.859-180del
XR_943842.1:n.954-2922del
XR_943843.1:n.954-2922del
NM_006939.3:c.859-180del	NP_008870.2:n.859-180del
NM_006939.4:c.859-180del MANE Select	NP_008870.2:n.859-180del