Canonical Allele Identifier: CA2136066055

Gene: SOS2

Linked Data

• dbSNP Id: rs1884711739
• gnomAD v4: 14-50153055-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153055C>A , CM000676.2:g.50153055C>A	GRCh38
NC_000014.8:g.50619773C>A , CM000676.1:g.50619773C>A	GRCh37
NC_000014.7:g.49689523C>A	NCBI36
NG_051073.1:g.83639G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2161+15G>T MANE Select	ENSP00000216373.5:n.2161+15G>T
ENST00000216373.9:c.2161+15G>T	ENSP00000216373.5:n.2161+15G>T
ENST00000543680.5:c.2062+15G>T	ENSP00000445328.1:n.2062+15G>T
NM_006939.2:c.2161+15G>T	NP_008870.2:n.2161+15G>T
XM_005268021.1:c.1981+15G>T	XP_005268078.1:n.1981+15G>T
XM_011537103.1:c.2122+15G>T	XP_011535405.1:n.2122+15G>T
XM_011537104.1:c.2161+15G>T	XP_011535406.1:n.2161+15G>T
NM_006939.3:c.2161+15G>T	NP_008870.2:n.2161+15G>T
NM_006939.4:c.2161+15G>T MANE Select	NP_008870.2:n.2161+15G>T