Canonical Allele Identifier: CA395871106

Gene: NOD2

Linked Data

• dbSNP Id: rs1444481596
• gnomAD v2: 16-50745973-G-C
• MyVariant Identifiers: chr16:g.50745973G>C (hg19) ; chr16:g.50712062G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50712062G>C , CM000678.2:g.50712062G>C	GRCh38
NC_000016.9:g.50745973G>C , CM000678.1:g.50745973G>C	GRCh37
NC_000016.8:g.49303474G>C	NCBI36
NG_007508.1:g.19924G>C , LRG_177:g.19924G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.2070G>C	ENSP00000493088.1:p.Lys690Asn
ENST00000646677.2:c.2070G>C	ENSP00000496533.1:p.Lys690Asn
ENST00000641284.1:c.2070G>C	ENSP00000493088.1:p.Lys690Asn
ENST00000646677.1:c.2070G>C	ENSP00000496533.1:p.Lys690Asn
ENST00000647318.2:c.2070G>C MANE Select	ENSP00000495993.1:p.Lys690Asn
ENST00000300589.6:c.2151G>C	ENSP00000300589.2:p.Lys717Asn
NM_001293557.1:c.2070G>C	NP_001280486.1:p.Lys690Asn
NM_022162.2:c.2151G>C	NP_071445.1:p.Lys717Asn
XM_005256084.2:c.2070G>C	XP_005256141.1:p.Lys690Asn
XM_006721242.2:c.2070G>C	XP_006721305.1:p.Lys690Asn
XM_006721243.2:c.2070G>C	XP_006721306.1:p.Lys690Asn
XM_011523257.1:c.1647G>C	XP_011521559.1:p.Lys549Asn
XM_011523258.1:c.1647G>C	XP_011521560.1:p.Lys549Asn
XM_011523259.1:c.1485G>C	XP_011521561.1:p.Lys495Asn
XM_011523260.1:c.2070G>C	XP_011521562.1:p.Lys690Asn
XM_011523261.1:c.2070G>C	XP_011521563.1:p.Lys690Asn
XR_429725.2:n.2160G>C
XR_429726.2:n.2160G>C
XR_933387.1:n.2160G>C
XM_005256084.4:c.2070G>C	XP_005256141.1:p.Lys690Asn
XM_006721242.4:c.2070G>C	XP_006721305.1:p.Lys690Asn
XM_006721243.4:c.2070G>C	XP_006721306.1:p.Lys690Asn
XM_011523259.2:c.1485G>C	XP_011521561.1:p.Lys495Asn
XM_011523260.3:c.2070G>C	XP_011521562.1:p.Lys690Asn
XM_011523261.2:c.2070G>C	XP_011521563.1:p.Lys690Asn
XM_017023535.1:c.1578G>C	XP_016879024.1:p.Lys526Asn
XM_017023536.1:c.1485G>C	XP_016879025.1:p.Lys495Asn
XM_017023537.1:c.1485G>C	XP_016879026.1:p.Lys495Asn
XM_017023538.1:c.1485G>C	XP_016879027.1:p.Lys495Asn
XR_429725.3:n.2113G>C
XR_429726.3:n.2113G>C
XR_933387.2:n.2113G>C
NM_001293557.2:c.2070G>C	NP_001280486.1:p.Lys690Asn
NM_001370466.1:c.2070G>C MANE Select	NP_001357395.1:p.Lys690Asn
NM_022162.3:c.2151G>C	NP_071445.1:p.Lys717Asn
NR_163434.1:n.2135G>C