Canonical Allele Identifier: CA254038911
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs939239901
MyVariant Identifiers: chr13:g.85032400G>A (hg19) chr13:g.84458265G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458265G>A , CM000675.2:g.84458265G>A GRCh38
NC_000013.10:g.85032400G>A , CM000675.1:g.85032400G>A GRCh37
NC_000013.9:g.83930401G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104099G>A
XR_942133.1:n.369-46346C>T
XR_942134.1:n.366-46346C>T
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