Canonical Allele Identifier: CA883820618
Gene: NLRP5 HGNC NCBI

Linked Data

dbSNP Id: rs1340768841
MyVariant Identifiers: chr19:g.56501088T>C (hg19) chr19:g.55989722T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55989722T>C , CM000681.2:g.55989722T>C GRCh38
NC_000019.9:g.56501088T>C , CM000681.1:g.56501088T>C GRCh37
NC_000019.8:g.61192900T>C NCBI36
NG_046924.1:g.7940T>C
NG_051553.1:g.46891T>C

Transcript Alleles

HGVS Amino-acid change
XM_011526444.1:c.-72+2901T>C XP_011524746.1:n.-72+2901T>C
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