Canonical Allele Identifier: CA191391286

Gene: LINGO2

Linked Data

• dbSNP Id: rs184490585
• gnomAD v2: 9-28011594-A-G
• gnomAD v3: 9-28011596-A-G
• gnomAD v4: 9-28011596-A-G
• MyVariant Identifiers: chr9:g.28011594A>G (hg19) ; chr9:g.28011596A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.28011596A>G , CM000671.2:g.28011596A>G	GRCh38
NC_000009.11:g.28011594A>G , CM000671.1:g.28011594A>G	GRCh37
NC_000009.10:g.28001594A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000698399.1:c.-35-60890T>C MANE Select	ENSP00000513694.1:n.-35-60890T>C
ENST00000698400.1:c.-36+14663T>C	ENSP00000513695.1:n.-36+14663T>C
ENST00000698401.1:c.-438-28238T>C	ENSP00000513696.1:n.-438-28238T>C
ENST00000698402.1:c.-35-60890T>C	ENSP00000513697.1:n.-35-60890T>C
ENST00000698403.1:c.-36+759T>C	ENSP00000513698.1:n.-36+759T>C
ENST00000698404.1:c.-36+759T>C	ENSP00000513699.1:n.-36+759T>C
ENST00000308675.5:c.-36+759T>C	ENSP00000310126.3:n.-36+759T>C
ENST00000379992.6:c.-36+759T>C	ENSP00000369328.1:n.-36+759T>C
ENST00000613945.3:c.-42-60883T>C	ENSP00000479634.1:n.-42-60883T>C
NM_001258282.1:c.-35-60890T>C	NP_001245211.1:n.-35-60890T>C
NM_152570.2:c.-36+759T>C	NP_689783.1:n.-36+759T>C
XM_005251372.3:c.-36+759T>C	XP_005251429.1:n.-36+759T>C
XM_011517715.1:c.-35-60890T>C	XP_011516017.1:n.-35-60890T>C
XM_011517716.1:c.-35-60890T>C	XP_011516018.1:n.-35-60890T>C
XM_011517717.1:c.-35-60890T>C	XP_011516019.1:n.-35-60890T>C
XM_011517718.1:c.-35-60890T>C	XP_011516020.1:n.-35-60890T>C
XM_011517719.1:c.-35-60890T>C	XP_011516021.1:n.-35-60890T>C
XM_011517720.1:c.-36+759T>C	XP_011516022.1:n.-36+759T>C
XM_011517721.1:c.-36+759T>C	XP_011516023.1:n.-36+759T>C
XM_011517722.1:c.-36+759T>C	XP_011516024.1:n.-36+759T>C
XM_011517723.1:c.-160+759T>C	XP_011516025.1:n.-160+759T>C
XM_011517724.1:c.-36+759T>C	XP_011516026.1:n.-36+759T>C
XM_011517725.1:c.-160+759T>C	XP_011516027.1:n.-160+759T>C
XM_011517726.1:c.-36+14136T>C	XP_011516028.1:n.-36+14136T>C
XM_011517727.1:c.-36+14663T>C	XP_011516029.1:n.-36+14663T>C
XM_011517728.1:c.-36+22527T>C	XP_011516030.1:n.-36+22527T>C
XM_011517729.1:c.-35-60890T>C	XP_011516031.1:n.-35-60890T>C
NM_001258282.2:c.-35-60890T>C	NP_001245211.1:n.-35-60890T>C
NM_001354574.1:c.-35-60890T>C	NP_001341503.1:n.-35-60890T>C
NM_001354575.1:c.-35-60890T>C	NP_001341504.1:n.-35-60890T>C
NM_152570.3:c.-36+759T>C	NP_689783.1:n.-36+759T>C
XM_011517724.2:c.-36+759T>C	XP_011516026.1:n.-36+759T>C
XM_011517728.2:c.-36+22527T>C	XP_011516030.1:n.-36+22527T>C
XM_017014303.2:c.-36+759T>C	XP_016869792.1:n.-36+759T>C
XM_017014304.1:c.-36+759T>C	XP_016869793.1:n.-36+759T>C
XM_017014305.1:c.-36+759T>C	XP_016869794.1:n.-36+759T>C
XM_017014306.2:c.-36+759T>C	XP_016869795.1:n.-36+759T>C
XR_001746186.2:n.2519-60890T>C
NM_001258282.3:c.-35-60890T>C MANE Select	NP_001245211.1:n.-35-60890T>C
NM_001354574.2:c.-35-60890T>C	NP_001341503.1:n.-35-60890T>C
NM_001354575.2:c.-35-60890T>C	NP_001341504.1:n.-35-60890T>C
NM_152570.4:c.-36+759T>C	NP_689783.1:n.-36+759T>C