Canonical Allele Identifier: CA2136066020

Gene: SOS2

Linked Data

• dbSNP Id: rs1884708781
• gnomAD v4: 14-50152974-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152976_50152978del , CM000676.2:g.50152976_50152978del	GRCh38
NC_000014.8:g.50619694_50619696del , CM000676.1:g.50619694_50619696del	GRCh37
NC_000014.7:g.49689444_49689446del	NCBI36
NG_051073.1:g.83717_83719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+93_2161+95del MANE Select	ENSP00000216373.5:n.2161+93_2161+95del
ENST00000216373.9:c.2161+93_2161+95del	ENSP00000216373.5:n.2161+93_2161+95del
ENST00000543680.5:c.2062+93_2062+95del	ENSP00000445328.1:n.2062+93_2062+95del
NM_006939.2:c.2161+93_2161+95del	NP_008870.2:n.2161+93_2161+95del
XM_005268021.1:c.1981+93_1981+95del	XP_005268078.1:n.1981+93_1981+95del
XM_011537103.1:c.2122+93_2122+95del	XP_011535405.1:n.2122+93_2122+95del
XM_011537104.1:c.2161+93_2161+95del	XP_011535406.1:n.2161+93_2161+95del
NM_006939.3:c.2161+93_2161+95del	NP_008870.2:n.2161+93_2161+95del
NM_006939.4:c.2161+93_2161+95del MANE Select	NP_008870.2:n.2161+93_2161+95del