Canonical Allele Identifier: CA2801534047

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152849C>A , CM000676.2:g.50152849C>A	GRCh38
NC_000014.8:g.50619567C>A , CM000676.1:g.50619567C>A	GRCh37
NC_000014.7:g.49689317C>A	NCBI36
NG_051073.1:g.83845G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+221G>T MANE Select	ENSP00000216373.5:n.2161+221G>T
ENST00000216373.9:c.2161+221G>T	ENSP00000216373.5:n.2161+221G>T
ENST00000543680.5:c.2062+221G>T	ENSP00000445328.1:n.2062+221G>T
NM_006939.2:c.2161+221G>T	NP_008870.2:n.2161+221G>T
XM_005268021.1:c.1981+221G>T	XP_005268078.1:n.1981+221G>T
XM_011537103.1:c.2122+221G>T	XP_011535405.1:n.2122+221G>T
XM_011537104.1:c.2161+221G>T	XP_011535406.1:n.2161+221G>T
NM_006939.3:c.2161+221G>T	NP_008870.2:n.2161+221G>T
NM_006939.4:c.2161+221G>T MANE Select	NP_008870.2:n.2161+221G>T