Canonical Allele Identifier: CA2136065992

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152931C= , CM000676.2:g.50152931C=	GRCh38
NC_000014.8:g.50619649C= , CM000676.1:g.50619649C=	GRCh37
NC_000014.7:g.49689399C=	NCBI36
NG_051073.1:g.83763G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+139G= MANE Select	ENSP00000216373.5:n.2161+139G=
ENST00000216373.9:c.2161+139G=	ENSP00000216373.5:n.2161+139G=
ENST00000543680.5:c.2062+139G=	ENSP00000445328.1:n.2062+139G=
NM_006939.2:c.2161+139G=	NP_008870.2:n.2161+139G=
XM_005268021.1:c.1981+139G=	XP_005268078.1:n.1981+139G=
XM_011537103.1:c.2122+139G=	XP_011535405.1:n.2122+139G=
XM_011537104.1:c.2161+139G=	XP_011535406.1:n.2161+139G=
NM_006939.3:c.2161+139G=	NP_008870.2:n.2161+139G=
NM_006939.4:c.2161+139G= MANE Select	NP_008870.2:n.2161+139G=