Canonical Allele Identifier: CA395868167
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50710986G>A , CM000678.2:g.50710986G>A GRCh38
NC_000016.9:g.50744897G>A , CM000678.1:g.50744897G>A GRCh37
NC_000016.8:g.49302398G>A NCBI36
NG_007508.1:g.18848G>A , LRG_177:g.18848G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.994G>A ENSP00000493088.1:p.Gly332Ser
ENST00000646677.2:c.994G>A ENSP00000496533.1:p.Gly332Ser
ENST00000641284.1:c.994G>A ENSP00000493088.1:p.Gly332Ser
ENST00000646677.1:c.994G>A ENSP00000496533.1:p.Gly332Ser
ENST00000647318.2:c.994G>A MANE Select ENSP00000495993.1:p.Gly332Ser
ENST00000300589.6:c.1075G>A ENSP00000300589.2:p.Gly359Ser
NM_001293557.1:c.994G>A NP_001280486.1:p.Gly332Ser
NM_022162.2:c.1075G>A NP_071445.1:p.Gly359Ser
XM_005256084.2:c.994G>A XP_005256141.1:p.Gly332Ser
XM_006721242.2:c.994G>A XP_006721305.1:p.Gly332Ser
XM_006721243.2:c.994G>A XP_006721306.1:p.Gly332Ser
XM_011523257.1:c.571G>A XP_011521559.1:p.Gly191Ser
XM_011523258.1:c.571G>A XP_011521560.1:p.Gly191Ser
XM_011523259.1:c.409G>A XP_011521561.1:p.Gly137Ser
XM_011523260.1:c.994G>A XP_011521562.1:p.Gly332Ser
XM_011523261.1:c.994G>A XP_011521563.1:p.Gly332Ser
XR_429725.2:n.1084G>A
XR_429726.2:n.1084G>A
XR_933387.1:n.1084G>A
XM_005256084.4:c.994G>A XP_005256141.1:p.Gly332Ser
XM_006721242.4:c.994G>A XP_006721305.1:p.Gly332Ser
XM_006721243.4:c.994G>A XP_006721306.1:p.Gly332Ser
XM_011523259.2:c.409G>A XP_011521561.1:p.Gly137Ser
XM_011523260.3:c.994G>A XP_011521562.1:p.Gly332Ser
XM_011523261.2:c.994G>A XP_011521563.1:p.Gly332Ser
XM_017023535.1:c.502G>A XP_016879024.1:p.Gly168Ser
XM_017023536.1:c.409G>A XP_016879025.1:p.Gly137Ser
XM_017023537.1:c.409G>A XP_016879026.1:p.Gly137Ser
XM_017023538.1:c.409G>A XP_016879027.1:p.Gly137Ser
XR_429725.3:n.1037G>A
XR_429726.3:n.1037G>A
XR_933387.2:n.1037G>A
NM_001293557.2:c.994G>A NP_001280486.1:p.Gly332Ser
NM_001370466.1:c.994G>A MANE Select NP_001357395.1:p.Gly332Ser
NM_022162.3:c.1075G>A NP_071445.1:p.Gly359Ser
NR_163434.1:n.1059G>A