Canonical Allele Identifier: CA2624771422

Gene: SOS2

Linked Data

• gnomAD v4: 14-50153050-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153050C>A , CM000676.2:g.50153050C>A	GRCh38
NC_000014.8:g.50619768C>A , CM000676.1:g.50619768C>A	GRCh37
NC_000014.7:g.49689518C>A	NCBI36
NG_051073.1:g.83644G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2161+20G>T MANE Select	ENSP00000216373.5:n.2161+20G>T
ENST00000216373.9:c.2161+20G>T	ENSP00000216373.5:n.2161+20G>T
ENST00000543680.5:c.2062+20G>T	ENSP00000445328.1:n.2062+20G>T
NM_006939.2:c.2161+20G>T	NP_008870.2:n.2161+20G>T
XM_005268021.1:c.1981+20G>T	XP_005268078.1:n.1981+20G>T
XM_011537103.1:c.2122+20G>T	XP_011535405.1:n.2122+20G>T
XM_011537104.1:c.2161+20G>T	XP_011535406.1:n.2161+20G>T
NM_006939.3:c.2161+20G>T	NP_008870.2:n.2161+20G>T
NM_006939.4:c.2161+20G>T MANE Select	NP_008870.2:n.2161+20G>T