Canonical Allele Identifier: CA15654870
Gene: LNCAROD HGNC NCBI

Linked Data

dbSNP Id: rs1733724
gnomAD v2: 10-54223977-A-G
gnomAD v3: 10-52464217-A-G
gnomAD v4: 10-52464217-A-G
MyVariant Identifiers: chr10:g.54223977A>G (hg19) chr10:g.52464217A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52464217A>G , CM000672.2:g.52464217A>G GRCh38
NC_000010.10:g.54223977A>G , CM000672.1:g.54223977A>G GRCh37
NC_000010.9:g.53893983A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120641.1:n.138-885T>C
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