Canonical Allele Identifier: CA150217

Gene: NOD2

Linked Data

• ClinVar Variation Id: 97834
• ClinVar RCV Id: RCV000084091 ; RCV002513872
• dbSNP Id: rs104895473
• gnomAD v4: 16-50711449-T-C
• MyVariant Identifiers: chr16:g.50745360T>C (hg19) ; chr16:g.50711449T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50711449T>C , CM000678.2:g.50711449T>C	GRCh38
NC_000016.9:g.50745360T>C , CM000678.1:g.50745360T>C	GRCh37
NC_000016.8:g.49302861T>C	NCBI36
NG_007508.1:g.19311T>C , LRG_177:g.19311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.1457T>C	ENSP00000493088.1:p.Met486Thr
ENST00000646677.2:c.1457T>C	ENSP00000496533.1:p.Met486Thr
ENST00000641284.1:c.1457T>C	ENSP00000493088.1:p.Met486Thr
ENST00000646677.1:c.1457T>C	ENSP00000496533.1:p.Met486Thr
ENST00000647318.2:c.1457T>C MANE Select	ENSP00000495993.1:p.Met486Thr
ENST00000300589.6:c.1538T>C	ENSP00000300589.2:p.Met513Thr
NM_001293557.1:c.1457T>C	NP_001280486.1:p.Met486Thr
NM_022162.2:c.1538T>C	NP_071445.1:p.Met513Thr
XM_005256084.2:c.1457T>C	XP_005256141.1:p.Met486Thr
XM_006721242.2:c.1457T>C	XP_006721305.1:p.Met486Thr
XM_006721243.2:c.1457T>C	XP_006721306.1:p.Met486Thr
XM_011523257.1:c.1034T>C	XP_011521559.1:p.Met345Thr
XM_011523258.1:c.1034T>C	XP_011521560.1:p.Met345Thr
XM_011523259.1:c.872T>C	XP_011521561.1:p.Met291Thr
XM_011523260.1:c.1457T>C	XP_011521562.1:p.Met486Thr
XM_011523261.1:c.1457T>C	XP_011521563.1:p.Met486Thr
XR_429725.2:n.1547T>C
XR_429726.2:n.1547T>C
XR_933387.1:n.1547T>C
XM_005256084.4:c.1457T>C	XP_005256141.1:p.Met486Thr
XM_006721242.4:c.1457T>C	XP_006721305.1:p.Met486Thr
XM_006721243.4:c.1457T>C	XP_006721306.1:p.Met486Thr
XM_011523259.2:c.872T>C	XP_011521561.1:p.Met291Thr
XM_011523260.3:c.1457T>C	XP_011521562.1:p.Met486Thr
XM_011523261.2:c.1457T>C	XP_011521563.1:p.Met486Thr
XM_017023535.1:c.965T>C	XP_016879024.1:p.Met322Thr
XM_017023536.1:c.872T>C	XP_016879025.1:p.Met291Thr
XM_017023537.1:c.872T>C	XP_016879026.1:p.Met291Thr
XM_017023538.1:c.872T>C	XP_016879027.1:p.Met291Thr
XR_429725.3:n.1500T>C
XR_429726.3:n.1500T>C
XR_933387.2:n.1500T>C
NM_001293557.2:c.1457T>C	NP_001280486.1:p.Met486Thr
NM_001370466.1:c.1457T>C MANE Select	NP_001357395.1:p.Met486Thr
NM_022162.3:c.1538T>C	NP_071445.1:p.Met513Thr
NR_163434.1:n.1522T>C