Canonical Allele Identifier: CA2801534061

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153037T>A , CM000676.2:g.50153037T>A	GRCh38
NC_000014.8:g.50619755T>A , CM000676.1:g.50619755T>A	GRCh37
NC_000014.7:g.49689505T>A	NCBI36
NG_051073.1:g.83657A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+33A>T MANE Select	ENSP00000216373.5:n.2161+33A>T
ENST00000216373.9:c.2161+33A>T	ENSP00000216373.5:n.2161+33A>T
ENST00000543680.5:c.2062+33A>T	ENSP00000445328.1:n.2062+33A>T
NM_006939.2:c.2161+33A>T	NP_008870.2:n.2161+33A>T
XM_005268021.1:c.1981+33A>T	XP_005268078.1:n.1981+33A>T
XM_011537103.1:c.2122+33A>T	XP_011535405.1:n.2122+33A>T
XM_011537104.1:c.2161+33A>T	XP_011535406.1:n.2161+33A>T
NM_006939.3:c.2161+33A>T	NP_008870.2:n.2161+33A>T
NM_006939.4:c.2161+33A>T MANE Select	NP_008870.2:n.2161+33A>T