Canonical Allele Identifier: CA16617533
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 421649
ClinVar RCV Id: RCV000487229
dbSNP Id: rs1064795274
MyVariant Identifiers: chr2:g.32476313C>T (hg19) chr2:g.32251244C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32251244C>T , CM000664.2:g.32251244C>T GRCh38
NC_000002.11:g.32476313C>T , CM000664.1:g.32476313C>T GRCh37
NC_000002.10:g.32329817C>T NCBI36
NG_041780.1:g.19500G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000652197.2:c.-76+5531G>A ENSP00000498301.2:n.-76+5531G>A
ENST00000402280.6:c.620G>A MANE Select ENSP00000385428.1:p.Arg207Lys
ENST00000404025.3:c.620G>A ENSP00000385090.3:p.Arg207Lys
ENST00000652197.1:c.620G>A ENSP00000498301.1:p.Arg207Lys
ENST00000342905.10:c.262+1175G>A ENSP00000339666.6:n.262+1175G>A
ENST00000360906.9:c.620G>A ENSP00000354159.5:p.Arg207Lys
ENST00000402280.5:c.620G>A ENSP00000385428.1:p.Arg207Lys
ENST00000404025.2:c.620G>A ENSP00000385090.2:p.Arg207Lys
NM_001199138.1:c.620G>A NP_001186067.1:p.Arg207Lys
NM_001199139.1:c.620G>A NP_001186068.1:p.Arg207Lys
NM_001302504.1:c.262+1175G>A NP_001289433.1:n.262+1175G>A
NM_021209.4:c.620G>A NP_067032.3:p.Arg207Lys
XM_011533008.1:c.620G>A XP_011531310.1:p.Arg207Lys
XM_017004619.1:c.620G>A XP_016860108.1:p.Arg207Lys
XR_001738872.1:n.881G>A
NM_001199138.2:c.620G>A MANE Select NP_001186067.1:p.Arg207Lys
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