Canonical Allele Identifier: CA10637859
Gene: NOD2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 319482
dbSNP Id: rs3135499

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50732216A>C , CM000678.2:g.50732216A>C GRCh38
NC_000016.9:g.50766127A>C , CM000678.1:g.50766127A>C GRCh37
NC_000016.8:g.49323628A>C NCBI36
NG_007508.1:g.40078A>C , LRG_177:g.40078A>C

Transcript Alleles

HGVS Amino-acid change
NM_001293557.1:c.*397A>C VV NP_001280486.1:p.=
NM_022162.2:c.*397A>C VV NP_071445.1:p.=
XM_005256084.2:c.*397A>C XP_005256141.1:p.=
XM_006721242.2:c.*397A>C XP_006721305.1:p.=
XM_011523257.1:c.*397A>C XP_011521559.1:p.=
XM_011523258.1:c.*397A>C XP_011521560.1:p.=
XM_011523259.1:c.*397A>C XP_011521561.1:p.=
XM_005256084.4:c.*397A>C XP_005256141.1:p.=
XM_006721242.4:c.*397A>C XP_006721305.1:p.=
XM_011523259.2:c.*397A>C XP_011521561.1:p.=
XM_017023535.1:c.*397A>C XP_016879024.1:p.=
XM_017023536.1:c.*397A>C XP_016879025.1:p.=
XM_017023537.1:c.*397A>C XP_016879026.1:p.=
XM_017023538.1:c.*397A>C XP_016879027.1:p.=
ENST00000300589.6:c.*397A>C ENSP00000300589.2:p.=