Canonical Allele Identifier: CA2575539880

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182434T>C , CM000676.2:g.50182434T>C	GRCh38
NC_000014.8:g.50649152T>C , CM000676.1:g.50649152T>C	GRCh37
NC_000014.7:g.49718902T>C	NCBI36
NG_051073.1:g.54260A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.858+29A>G MANE Select	ENSP00000216373.5:n.858+29A>G
ENST00000216373.9:c.858+29A>G	ENSP00000216373.5:n.858+29A>G
ENST00000543680.5:c.858+29A>G	ENSP00000445328.1:n.858+29A>G
NM_006939.2:c.858+29A>G	NP_008870.2:n.858+29A>G
XM_005268021.1:c.678+29A>G	XP_005268078.1:n.678+29A>G
XM_011537103.1:c.819+29A>G	XP_011535405.1:n.819+29A>G
XM_011537104.1:c.858+29A>G	XP_011535406.1:n.858+29A>G
XR_943842.1:n.954-1353T>C
XR_943843.1:n.954-1353T>C
NM_006939.3:c.858+29A>G	NP_008870.2:n.858+29A>G
NM_006939.4:c.858+29A>G MANE Select	NP_008870.2:n.858+29A>G