Canonical Allele Identifier: CA2624772933

Gene: SOS2

Linked Data

• gnomAD v4: 14-50182418-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182418G>T , CM000676.2:g.50182418G>T	GRCh38
NC_000014.8:g.50649136G>T , CM000676.1:g.50649136G>T	GRCh37
NC_000014.7:g.49718886G>T	NCBI36
NG_051073.1:g.54276C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.858+45C>A MANE Select	ENSP00000216373.5:n.858+45C>A
ENST00000216373.9:c.858+45C>A	ENSP00000216373.5:n.858+45C>A
ENST00000543680.5:c.858+45C>A	ENSP00000445328.1:n.858+45C>A
NM_006939.2:c.858+45C>A	NP_008870.2:n.858+45C>A
XM_005268021.1:c.678+45C>A	XP_005268078.1:n.678+45C>A
XM_011537103.1:c.819+45C>A	XP_011535405.1:n.819+45C>A
XM_011537104.1:c.858+45C>A	XP_011535406.1:n.858+45C>A
XR_943842.1:n.954-1369G>T
XR_943843.1:n.954-1369G>T
NM_006939.3:c.858+45C>A	NP_008870.2:n.858+45C>A
NM_006939.4:c.858+45C>A MANE Select	NP_008870.2:n.858+45C>A