Canonical Allele Identifier: CA701680076
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1356892935
MyVariant Identifiers: chr13:g.85032167T>C (hg19) chr13:g.84458032T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458032T>C , CM000675.2:g.84458032T>C GRCh38
NC_000013.10:g.85032167T>C , CM000675.1:g.85032167T>C GRCh37
NC_000013.9:g.83930168T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104332T>C
XR_942133.1:n.369-46113A>G
XR_942134.1:n.366-46113A>G
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