Canonical Allele Identifier: CA254038900
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs956704083
gnomAD v2: 13-85032299-A-G
gnomAD v3: 13-84458164-A-G
gnomAD v4: 13-84458164-A-G
MyVariant Identifiers: chr13:g.85032299A>G (hg19) chr13:g.84458164A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458164A>G , CM000675.2:g.84458164A>G GRCh38
NC_000013.10:g.85032299A>G , CM000675.1:g.85032299A>G GRCh37
NC_000013.9:g.83930300A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104200A>G
XR_942133.1:n.369-46245T>C
XR_942134.1:n.366-46245T>C
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