Canonical Allele Identifier: CA706566948

Gene: SOS2

Linked Data

• dbSNP Id: rs1195919628
• gnomAD v3: 14-50180747-AG-A
• gnomAD v4: 14-50180747-AG-A
• MyVariant Identifiers: chr14:g.50647466del (hg19) ; chr14:g.50180748del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180748del , CM000676.2:g.50180748del	GRCh38
NC_000014.8:g.50647466del , CM000676.1:g.50647466del	GRCh37
NC_000014.7:g.49717216del	NCBI36
NG_051073.1:g.55946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-66del MANE Select	ENSP00000216373.5:n.859-66del
ENST00000216373.9:c.859-66del	ENSP00000216373.5:n.859-66del
ENST00000543680.5:c.859-66del	ENSP00000445328.1:n.859-66del
NM_006939.2:c.859-66del	NP_008870.2:n.859-66del
XM_005268021.1:c.679-66del	XP_005268078.1:n.679-66del
XM_011537103.1:c.820-66del	XP_011535405.1:n.820-66del
XM_011537104.1:c.859-66del	XP_011535406.1:n.859-66del
XR_943842.1:n.954-3039del
XR_943843.1:n.954-3039del
NM_006939.3:c.859-66del	NP_008870.2:n.859-66del
NM_006939.4:c.859-66del MANE Select	NP_008870.2:n.859-66del