Canonical Allele Identifier: CA2136084789

Gene: SOS2

Linked Data

• dbSNP Id: rs1039608156
• gnomAD v4: 14-50180775-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180775C>G , CM000676.2:g.50180775C>G	GRCh38
NC_000014.8:g.50647493C>G , CM000676.1:g.50647493C>G	GRCh37
NC_000014.7:g.49717243C>G	NCBI36
NG_051073.1:g.55919G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-93G>C MANE Select	ENSP00000216373.5:n.859-93G>C
ENST00000216373.9:c.859-93G>C	ENSP00000216373.5:n.859-93G>C
ENST00000543680.5:c.859-93G>C	ENSP00000445328.1:n.859-93G>C
NM_006939.2:c.859-93G>C	NP_008870.2:n.859-93G>C
XM_005268021.1:c.679-93G>C	XP_005268078.1:n.679-93G>C
XM_011537103.1:c.820-93G>C	XP_011535405.1:n.820-93G>C
XM_011537104.1:c.859-93G>C	XP_011535406.1:n.859-93G>C
XR_943842.1:n.954-3012C>G
XR_943843.1:n.954-3012C>G
NM_006939.3:c.859-93G>C	NP_008870.2:n.859-93G>C
NM_006939.4:c.859-93G>C MANE Select	NP_008870.2:n.859-93G>C