Canonical Allele Identifier: CA395876772

Gene: NOD2

Linked Data

• dbSNP Id: rs1486037435
• gnomAD v2: 16-50763765-A-T
• gnomAD v4: 16-50729854-A-T
• MyVariant Identifiers: chr16:g.50763765A>T (hg19) ; chr16:g.50729854A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729854A>T , CM000678.2:g.50729854A>T	GRCh38
NC_000016.9:g.50763765A>T , CM000678.1:g.50763765A>T	GRCh37
NC_000016.8:g.49321266A>T	NCBI36
NG_007508.1:g.37716A>T , LRG_177:g.37716A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.*36A>T	ENSP00000493088.1:n.*36A>T
ENST00000646677.2:c.*687A>T	ENSP00000496533.1:n.*687A>T
ENST00000697428.1:n.2400A>T
ENST00000641284.1:c.*36A>T	ENSP00000493088.1:n.*36A>T
ENST00000646677.1:c.*687A>T	ENSP00000496533.1:n.*687A>T
ENST00000647318.2:c.2922A>T MANE Select	ENSP00000495993.1:p.Glu974Asp
ENST00000300589.6:c.3003A>T	ENSP00000300589.2:p.Glu1001Asp
NM_001293557.1:c.2922A>T	NP_001280486.1:p.Glu974Asp
NM_022162.2:c.3003A>T	NP_071445.1:p.Glu1001Asp
XM_005256084.2:c.2922A>T	XP_005256141.1:p.Glu974Asp
XM_006721242.2:c.2838A>T	XP_006721305.1:p.Glu946Asp
XM_011523257.1:c.2499A>T	XP_011521559.1:p.Glu833Asp
XM_011523258.1:c.2499A>T	XP_011521560.1:p.Glu833Asp
XM_011523259.1:c.2337A>T	XP_011521561.1:p.Glu779Asp
XM_005256084.4:c.2922A>T	XP_005256141.1:p.Glu974Asp
XM_006721242.4:c.2838A>T	XP_006721305.1:p.Glu946Asp
XM_011523259.2:c.2337A>T	XP_011521561.1:p.Glu779Asp
XM_017023535.1:c.2430A>T	XP_016879024.1:p.Glu810Asp
XM_017023536.1:c.2337A>T	XP_016879025.1:p.Glu779Asp
XM_017023537.1:c.2337A>T	XP_016879026.1:p.Glu779Asp
XM_017023538.1:c.2337A>T	XP_016879027.1:p.Glu779Asp
NM_001293557.2:c.2922A>T	NP_001280486.1:p.Glu974Asp
NM_001370466.1:c.2922A>T MANE Select	NP_001357395.1:p.Glu974Asp
NM_022162.3:c.3003A>T	NP_071445.1:p.Glu1001Asp
NR_163434.1:n.3134A>T