Canonical Allele Identifier: CA2136066039

Gene: SOS2

Linked Data

• dbSNP Id: rs1884710554

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153028C>G , CM000676.2:g.50153028C>G	GRCh38
NC_000014.8:g.50619746C>G , CM000676.1:g.50619746C>G	GRCh37
NC_000014.7:g.49689496C>G	NCBI36
NG_051073.1:g.83666G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2161+42G>C MANE Select	ENSP00000216373.5:n.2161+42G>C
ENST00000216373.9:c.2161+42G>C	ENSP00000216373.5:n.2161+42G>C
ENST00000543680.5:c.2062+42G>C	ENSP00000445328.1:n.2062+42G>C
NM_006939.2:c.2161+42G>C	NP_008870.2:n.2161+42G>C
XM_005268021.1:c.1981+42G>C	XP_005268078.1:n.1981+42G>C
XM_011537103.1:c.2122+42G>C	XP_011535405.1:n.2122+42G>C
XM_011537104.1:c.2161+42G>C	XP_011535406.1:n.2161+42G>C
NM_006939.3:c.2161+42G>C	NP_008870.2:n.2161+42G>C
NM_006939.4:c.2161+42G>C MANE Select	NP_008870.2:n.2161+42G>C