Canonical Allele Identifier: CA963009056

Gene: SOS2

Linked Data

• gnomAD v3: 14-50180842-C-A
• gnomAD v4: 14-50180842-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180842C>A , CM000676.2:g.50180842C>A	GRCh38
NC_000014.8:g.50647560C>A , CM000676.1:g.50647560C>A	GRCh37
NC_000014.7:g.49717310C>A	NCBI36
NG_051073.1:g.55852G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-160G>T MANE Select	ENSP00000216373.5:n.859-160G>T
ENST00000216373.9:c.859-160G>T	ENSP00000216373.5:n.859-160G>T
ENST00000543680.5:c.859-160G>T	ENSP00000445328.1:n.859-160G>T
NM_006939.2:c.859-160G>T	NP_008870.2:n.859-160G>T
XM_005268021.1:c.679-160G>T	XP_005268078.1:n.679-160G>T
XM_011537103.1:c.820-160G>T	XP_011535405.1:n.820-160G>T
XM_011537104.1:c.859-160G>T	XP_011535406.1:n.859-160G>T
XR_943842.1:n.954-2945C>A
XR_943843.1:n.954-2945C>A
NM_006939.3:c.859-160G>T	NP_008870.2:n.859-160G>T
NM_006939.4:c.859-160G>T MANE Select	NP_008870.2:n.859-160G>T