Canonical Allele Identifier: CA150265
Gene: NOD2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 97851
dbSNP Id: rs104895444

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50712288G>A , CM000678.2:g.50712288G>A GRCh38
NC_000016.9:g.50746199G>A , CM000678.1:g.50746199G>A GRCh37
NC_000016.8:g.49303700G>A NCBI36
NG_007508.1:g.20150G>A , LRG_177:g.20150G>A

Transcript Alleles

HGVS Amino-acid change
NM_001293557.1:c.2296G>A VV NP_001280486.1:p.Val766Met
NM_022162.2:c.2377G>A VV NP_071445.1:p.Val793Met
XM_005256084.2:c.2296G>A XP_005256141.1:p.Val766Met
XM_006721242.2:c.2296G>A XP_006721305.1:p.Val766Met
XM_006721243.2:c.2296G>A XP_006721306.1:p.Val766Met
XM_011523257.1:c.1873G>A XP_011521559.1:p.Val625Met
XM_011523258.1:c.1873G>A XP_011521560.1:p.Val625Met
XM_011523259.1:c.1711G>A XP_011521561.1:p.Val571Met
XM_011523260.1:c.2296G>A XP_011521562.1:p.Val766Met
XM_011523261.1:c.2296G>A XP_011521563.1:p.Val766Met
XR_429725.2:n.2386G>A
XR_429726.2:n.2386G>A
XR_933387.1:n.2386G>A
XM_005256084.4:c.2296G>A
XM_006721242.4:c.2296G>A
XM_006721243.4:c.2296G>A
XM_011523259.2:c.1711G>A
XM_011523260.3:c.2296G>A
XM_011523261.2:c.2296G>A
XM_017023535.1:c.1804G>A XP_016879024.1:p.Val602Met
XM_017023536.1:c.1711G>A XP_016879025.1:p.Val571Met
XM_017023537.1:c.1711G>A XP_016879026.1:p.Val571Met
XM_017023538.1:c.1711G>A XP_016879027.1:p.Val571Met
XR_429725.3:n.2339G>A
XR_429726.3:n.2339G>A
XR_933387.2:n.2339G>A
ENST00000300589.6:c.2377G>A ENSP00000300589.2:p.Val793Met
ENST00000524712.5:n.95G>A
ENST00000527052.5:n.95G>A
ENST00000529633.5:n.95G>A
ENST00000534057.1:n.95G>A
ENST00000534067.5:n.95G>A