Canonical Allele Identifier: CA2136039808

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150246A= , CM000676.2:g.50150246A=	GRCh38
NC_000014.8:g.50616964A= , CM000676.1:g.50616964A=	GRCh37
NC_000014.7:g.49686714A=	NCBI36
NG_051073.1:g.86448T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2162-16T= MANE Select	ENSP00000216373.5:n.2162-16T=
ENST00000216373.9:c.2162-16T=	ENSP00000216373.5:n.2162-16T=
ENST00000543680.5:c.2063-16T=	ENSP00000445328.1:n.2063-16T=
NM_006939.2:c.2162-16T=	NP_008870.2:n.2162-16T=
XM_005268021.1:c.1982-16T=	XP_005268078.1:n.1982-16T=
XM_011537103.1:c.2123-16T=	XP_011535405.1:n.2123-16T=
XM_011537104.1:c.2162-16T=	XP_011535406.1:n.2162-16T=
NM_006939.3:c.2162-16T=	NP_008870.2:n.2162-16T=
NM_006939.4:c.2162-16T= MANE Select	NP_008870.2:n.2162-16T=