Canonical Allele Identifier: CA2624773387

Gene: SOS2

Linked Data

• gnomAD v4: 14-50199886-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199886A>C , CM000676.2:g.50199886A>C	GRCh38
NC_000014.8:g.50666604A>C , CM000676.1:g.50666604A>C	GRCh37
NC_000014.7:g.49736354A>C	NCBI36
NG_051073.1:g.36808T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.346-31T>G MANE Select	ENSP00000216373.5:n.346-31T>G
ENST00000216373.9:c.346-31T>G	ENSP00000216373.5:n.346-31T>G
ENST00000543680.5:c.346-31T>G	ENSP00000445328.1:n.346-31T>G
ENST00000555666.1:n.525-31T>G
ENST00000556469.5:n.317-31T>G
NM_006939.2:c.346-31T>G	NP_008870.2:n.346-31T>G
XM_005268021.1:c.166-31T>G	XP_005268078.1:n.166-31T>G
XM_011537103.1:c.307-31T>G	XP_011535405.1:n.307-31T>G
XM_011537104.1:c.346-31T>G	XP_011535406.1:n.346-31T>G
XR_943842.1:n.1039+16014A>C
XR_943843.1:n.1039+16014A>C
NM_006939.3:c.346-31T>G	NP_008870.2:n.346-31T>G
NM_006939.4:c.346-31T>G MANE Select	NP_008870.2:n.346-31T>G