Canonical Allele Identifier: CA2624772513

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180711-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180711A>G , CM000676.2:g.50180711A>G	GRCh38
NC_000014.8:g.50647429A>G , CM000676.1:g.50647429A>G	GRCh37
NC_000014.7:g.49717179A>G	NCBI36
NG_051073.1:g.55983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-29T>C MANE Select	ENSP00000216373.5:n.859-29T>C
ENST00000216373.9:c.859-29T>C	ENSP00000216373.5:n.859-29T>C
ENST00000543680.5:c.859-29T>C	ENSP00000445328.1:n.859-29T>C
NM_006939.2:c.859-29T>C	NP_008870.2:n.859-29T>C
XM_005268021.1:c.679-29T>C	XP_005268078.1:n.679-29T>C
XM_011537103.1:c.820-29T>C	XP_011535405.1:n.820-29T>C
XM_011537104.1:c.859-29T>C	XP_011535406.1:n.859-29T>C
XR_943842.1:n.954-3076A>G
XR_943843.1:n.954-3076A>G
NM_006939.3:c.859-29T>C	NP_008870.2:n.859-29T>C
NM_006939.4:c.859-29T>C MANE Select	NP_008870.2:n.859-29T>C