Canonical Allele Identifier: CA2624771871

Gene: SOS2

Linked Data

• gnomAD v4: 14-50180466-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180466G>A , CM000676.2:g.50180466G>A	GRCh38
NC_000014.8:g.50647184G>A , CM000676.1:g.50647184G>A	GRCh37
NC_000014.7:g.49716934G>A	NCBI36
NG_051073.1:g.56228C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.969+106C>T MANE Select	ENSP00000216373.5:n.969+106C>T
ENST00000216373.9:c.969+106C>T	ENSP00000216373.5:n.969+106C>T
ENST00000543680.5:c.969+106C>T	ENSP00000445328.1:n.969+106C>T
ENST00000555794.2:c.83+106C>T
NM_006939.2:c.969+106C>T	NP_008870.2:n.969+106C>T
XM_005268021.1:c.789+106C>T	XP_005268078.1:n.789+106C>T
XM_011537103.1:c.930+106C>T	XP_011535405.1:n.930+106C>T
XM_011537104.1:c.969+106C>T	XP_011535406.1:n.969+106C>T
XR_943842.1:n.954-3321G>A
XR_943843.1:n.954-3321G>A
NM_006939.3:c.969+106C>T	NP_008870.2:n.969+106C>T
NM_006939.4:c.969+106C>T MANE Select	NP_008870.2:n.969+106C>T