Canonical Allele Identifier: CA8051412
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319439
dbSNP Id: rs560242309

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50710770C>T , CM000678.2:g.50710770C>T GRCh38
NC_000016.9:g.50744681C>T , CM000678.1:g.50744681C>T GRCh37
NC_000016.8:g.49302182C>T NCBI36
NG_007508.1:g.18632C>T , LRG_177:g.18632C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.778C>T ENSP00000493088.1:p.His260Tyr
ENST00000646677.2:c.778C>T ENSP00000496533.1:p.His260Tyr
ENST00000641284.1:c.778C>T ENSP00000493088.1:p.His260Tyr
ENST00000646677.1:c.778C>T ENSP00000496533.1:p.His260Tyr
ENST00000647318.2:c.778C>T MANE Select ENSP00000495993.1:p.His260Tyr
ENST00000300589.6:c.859C>T ENSP00000300589.2:p.His287Tyr
ENST00000526417.6:n.919C>T
ENST00000527070.5:c.*1474C>T ENSP00000435149.1:n.*1474C>T
ENST00000532206.1:n.857C>T
NM_001293557.1:c.778C>T NP_001280486.1:p.His260Tyr
NM_022162.2:c.859C>T NP_071445.1:p.His287Tyr
XM_005256084.2:c.778C>T XP_005256141.1:p.His260Tyr
XM_006721242.2:c.778C>T XP_006721305.1:p.His260Tyr
XM_006721243.2:c.778C>T XP_006721306.1:p.His260Tyr
XM_011523257.1:c.355C>T XP_011521559.1:p.His119Tyr
XM_011523258.1:c.355C>T XP_011521560.1:p.His119Tyr
XM_011523259.1:c.193C>T XP_011521561.1:p.His65Tyr
XM_011523260.1:c.778C>T XP_011521562.1:p.His260Tyr
XM_011523261.1:c.778C>T XP_011521563.1:p.His260Tyr
XR_429725.2:n.868C>T
XR_429726.2:n.868C>T
XR_933387.1:n.868C>T
XM_005256084.4:c.778C>T XP_005256141.1:p.His260Tyr
XM_006721242.4:c.778C>T XP_006721305.1:p.His260Tyr
XM_006721243.4:c.778C>T XP_006721306.1:p.His260Tyr
XM_011523259.2:c.193C>T XP_011521561.1:p.His65Tyr
XM_011523260.3:c.778C>T XP_011521562.1:p.His260Tyr
XM_011523261.2:c.778C>T XP_011521563.1:p.His260Tyr
XM_017023535.1:c.286C>T XP_016879024.1:p.His96Tyr
XM_017023536.1:c.193C>T XP_016879025.1:p.His65Tyr
XM_017023537.1:c.193C>T XP_016879026.1:p.His65Tyr
XM_017023538.1:c.193C>T XP_016879027.1:p.His65Tyr
XR_429725.3:n.821C>T
XR_429726.3:n.821C>T
XR_933387.2:n.821C>T
NM_001293557.2:c.778C>T NP_001280486.1:p.His260Tyr
NM_001370466.1:c.778C>T MANE Select NP_001357395.1:p.His260Tyr
NM_022162.3:c.859C>T NP_071445.1:p.His287Tyr
NR_163434.1:n.843C>T