Canonical Allele Identifier: CA310249720
Gene: NLRP5 HGNC NCBI

Linked Data

dbSNP Id: rs527930468
gnomAD v3: 19-55989519-C-T
gnomAD v4: 19-55989519-C-T
MyVariant Identifiers: chr19:g.56500885C>T (hg19) chr19:g.55989519C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55989519C>T , CM000681.2:g.55989519C>T GRCh38
NC_000019.9:g.56500885C>T , CM000681.1:g.56500885C>T GRCh37
NC_000019.8:g.61192697C>T NCBI36
NG_046924.1:g.7737C>T
NG_051553.1:g.46688C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011526444.1:c.-72+2698C>T XP_011524746.1:n.-72+2698C>T
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