Canonical Allele Identifier: CA495779022
Gene: NOD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.50746021G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50712110G>A , CM000678.2:g.50712110G>A GRCh38
NC_000016.9:g.50746021G>A , CM000678.1:g.50746021G>A GRCh37
NC_000016.8:g.49303522G>A NCBI36
NG_007508.1:g.19972G>A , LRG_177:g.19972G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.2118G>A ENSP00000493088.1:p.Val706=
ENST00000646677.2:c.2118G>A ENSP00000496533.1:p.Val706=
ENST00000641284.1:c.2118G>A ENSP00000493088.1:p.Val706=
ENST00000646677.1:c.2118G>A ENSP00000496533.1:p.Val706=
ENST00000647318.2:c.2118G>A MANE Select ENSP00000495993.1:p.Val706=
ENST00000300589.6:c.2199G>A ENSP00000300589.2:p.Val733=
NM_001293557.1:c.2118G>A NP_001280486.1:p.Val706=
NM_022162.2:c.2199G>A NP_071445.1:p.Val733=
XM_005256084.2:c.2118G>A XP_005256141.1:p.Val706=
XM_006721242.2:c.2118G>A XP_006721305.1:p.Val706=
XM_006721243.2:c.2118G>A XP_006721306.1:p.Val706=
XM_011523257.1:c.1695G>A XP_011521559.1:p.Val565=
XM_011523258.1:c.1695G>A XP_011521560.1:p.Val565=
XM_011523259.1:c.1533G>A XP_011521561.1:p.Val511=
XM_011523260.1:c.2118G>A XP_011521562.1:p.Val706=
XM_011523261.1:c.2118G>A XP_011521563.1:p.Val706=
XR_429725.2:n.2208G>A
XR_429726.2:n.2208G>A
XR_933387.1:n.2208G>A
XM_005256084.4:c.2118G>A XP_005256141.1:p.Val706=
XM_006721242.4:c.2118G>A XP_006721305.1:p.Val706=
XM_006721243.4:c.2118G>A XP_006721306.1:p.Val706=
XM_011523259.2:c.1533G>A XP_011521561.1:p.Val511=
XM_011523260.3:c.2118G>A XP_011521562.1:p.Val706=
XM_011523261.2:c.2118G>A XP_011521563.1:p.Val706=
XM_017023535.1:c.1626G>A XP_016879024.1:p.Val542=
XM_017023536.1:c.1533G>A XP_016879025.1:p.Val511=
XM_017023537.1:c.1533G>A XP_016879026.1:p.Val511=
XM_017023538.1:c.1533G>A XP_016879027.1:p.Val511=
XR_429725.3:n.2161G>A
XR_429726.3:n.2161G>A
XR_933387.2:n.2161G>A
NM_001293557.2:c.2118G>A NP_001280486.1:p.Val706=
NM_001370466.1:c.2118G>A MANE Select NP_001357395.1:p.Val706=
NM_022162.3:c.2199G>A NP_071445.1:p.Val733=
NR_163434.1:n.2183G>A