Canonical Allele Identifier: CA2136084771

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180765C= , CM000676.2:g.50180765C=	GRCh38
NC_000014.8:g.50647483C= , CM000676.1:g.50647483C=	GRCh37
NC_000014.7:g.49717233C=	NCBI36
NG_051073.1:g.55929G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-83G= MANE Select	ENSP00000216373.5:n.859-83G=
ENST00000216373.9:c.859-83G=	ENSP00000216373.5:n.859-83G=
ENST00000543680.5:c.859-83G=	ENSP00000445328.1:n.859-83G=
NM_006939.2:c.859-83G=	NP_008870.2:n.859-83G=
XM_005268021.1:c.679-83G=	XP_005268078.1:n.679-83G=
XM_011537103.1:c.820-83G=	XP_011535405.1:n.820-83G=
XM_011537104.1:c.859-83G=	XP_011535406.1:n.859-83G=
XR_943842.1:n.954-3022C=
XR_943843.1:n.954-3022C=
NM_006939.3:c.859-83G=	NP_008870.2:n.859-83G=
NM_006939.4:c.859-83G= MANE Select	NP_008870.2:n.859-83G=