Canonical Allele Identifier: CA395867502

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50744580C>G (hg19) ; chr16:g.50710669C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50710669C>G , CM000678.2:g.50710669C>G	GRCh38
NC_000016.9:g.50744580C>G , CM000678.1:g.50744580C>G	GRCh37
NC_000016.8:g.49302081C>G	NCBI36
NG_007508.1:g.18531C>G , LRG_177:g.18531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.677C>G	ENSP00000493088.1:p.Thr226Arg
ENST00000646677.2:c.677C>G	ENSP00000496533.1:p.Thr226Arg
ENST00000641284.1:c.677C>G	ENSP00000493088.1:p.Thr226Arg
ENST00000646677.1:c.677C>G	ENSP00000496533.1:p.Thr226Arg
ENST00000647318.2:c.677C>G MANE Select	ENSP00000495993.1:p.Thr226Arg
ENST00000300589.6:c.758C>G	ENSP00000300589.2:p.Thr253Arg
ENST00000526417.6:n.818C>G
ENST00000527070.5:c.*1373C>G	ENSP00000435149.1:n.*1373C>G
ENST00000532206.1:n.756C>G
NM_001293557.1:c.677C>G	NP_001280486.1:p.Thr226Arg
NM_022162.2:c.758C>G	NP_071445.1:p.Thr253Arg
XM_005256084.2:c.677C>G	XP_005256141.1:p.Thr226Arg
XM_006721242.2:c.677C>G	XP_006721305.1:p.Thr226Arg
XM_006721243.2:c.677C>G	XP_006721306.1:p.Thr226Arg
XM_011523257.1:c.254C>G	XP_011521559.1:p.Thr85Arg
XM_011523258.1:c.254C>G	XP_011521560.1:p.Thr85Arg
XM_011523259.1:c.92C>G	XP_011521561.1:p.Thr31Arg
XM_011523260.1:c.677C>G	XP_011521562.1:p.Thr226Arg
XM_011523261.1:c.677C>G	XP_011521563.1:p.Thr226Arg
XR_429725.2:n.767C>G
XR_429726.2:n.767C>G
XR_933387.1:n.767C>G
XM_005256084.4:c.677C>G	XP_005256141.1:p.Thr226Arg
XM_006721242.4:c.677C>G	XP_006721305.1:p.Thr226Arg
XM_006721243.4:c.677C>G	XP_006721306.1:p.Thr226Arg
XM_011523259.2:c.92C>G	XP_011521561.1:p.Thr31Arg
XM_011523260.3:c.677C>G	XP_011521562.1:p.Thr226Arg
XM_011523261.2:c.677C>G	XP_011521563.1:p.Thr226Arg
XM_017023535.1:c.185C>G	XP_016879024.1:p.Thr62Arg
XM_017023536.1:c.92C>G	XP_016879025.1:p.Thr31Arg
XM_017023537.1:c.92C>G	XP_016879026.1:p.Thr31Arg
XM_017023538.1:c.92C>G	XP_016879027.1:p.Thr31Arg
XR_429725.3:n.720C>G
XR_429726.3:n.720C>G
XR_933387.2:n.720C>G
NM_001293557.2:c.677C>G	NP_001280486.1:p.Thr226Arg
NM_001370466.1:c.677C>G MANE Select	NP_001357395.1:p.Thr226Arg
NM_022162.3:c.758C>G	NP_071445.1:p.Thr253Arg
NR_163434.1:n.742C>G