Canonical Allele Identifier: CA8051380

Gene: NOD2

Linked Data

• dbSNP Id: rs768859303
• ExAC: 16:50744536 T / C
• gnomAD v2: 16-50744536-T-C
• gnomAD v3: 16-50710625-T-C
• gnomAD v4: 16-50710625-T-C
• MyVariant Identifiers: chr16:g.50744536T>C (hg19) ; chr16:g.50710625T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50710625T>C , CM000678.2:g.50710625T>C	GRCh38
NC_000016.9:g.50744536T>C , CM000678.1:g.50744536T>C	GRCh37
NC_000016.8:g.49302037T>C	NCBI36
NG_007508.1:g.18487T>C , LRG_177:g.18487T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.633T>C	ENSP00000493088.1:p.Ser211=
ENST00000646677.2:c.633T>C	ENSP00000496533.1:p.Ser211=
ENST00000641284.1:c.633T>C	ENSP00000493088.1:p.Ser211=
ENST00000646677.1:c.633T>C	ENSP00000496533.1:p.Ser211=
ENST00000647318.2:c.633T>C MANE Select	ENSP00000495993.1:p.Ser211=
ENST00000300589.6:c.714T>C	ENSP00000300589.2:p.Ser238=
ENST00000526417.6:n.774T>C
ENST00000527070.5:c.*1329T>C	ENSP00000435149.1:n.*1329T>C
ENST00000532206.1:n.712T>C
NM_001293557.1:c.633T>C	NP_001280486.1:p.Ser211=
NM_022162.2:c.714T>C	NP_071445.1:p.Ser238=
XM_005256084.2:c.633T>C	XP_005256141.1:p.Ser211=
XM_006721242.2:c.633T>C	XP_006721305.1:p.Ser211=
XM_006721243.2:c.633T>C	XP_006721306.1:p.Ser211=
XM_011523257.1:c.210T>C	XP_011521559.1:p.Ser70=
XM_011523258.1:c.210T>C	XP_011521560.1:p.Ser70=
XM_011523259.1:c.48T>C	XP_011521561.1:p.Ser16=
XM_011523260.1:c.633T>C	XP_011521562.1:p.Ser211=
XM_011523261.1:c.633T>C	XP_011521563.1:p.Ser211=
XR_429725.2:n.723T>C
XR_429726.2:n.723T>C
XR_933387.1:n.723T>C
XM_005256084.4:c.633T>C	XP_005256141.1:p.Ser211=
XM_006721242.4:c.633T>C	XP_006721305.1:p.Ser211=
XM_006721243.4:c.633T>C	XP_006721306.1:p.Ser211=
XM_011523259.2:c.48T>C	XP_011521561.1:p.Ser16=
XM_011523260.3:c.633T>C	XP_011521562.1:p.Ser211=
XM_011523261.2:c.633T>C	XP_011521563.1:p.Ser211=
XM_017023535.1:c.141T>C	XP_016879024.1:p.Ser47=
XM_017023536.1:c.48T>C	XP_016879025.1:p.Ser16=
XM_017023537.1:c.48T>C	XP_016879026.1:p.Ser16=
XM_017023538.1:c.48T>C	XP_016879027.1:p.Ser16=
XR_429725.3:n.676T>C
XR_429726.3:n.676T>C
XR_933387.2:n.676T>C
NM_001293557.2:c.633T>C	NP_001280486.1:p.Ser211=
NM_001370466.1:c.633T>C MANE Select	NP_001357395.1:p.Ser211=
NM_022162.3:c.714T>C	NP_071445.1:p.Ser238=
NR_163434.1:n.698T>C