Canonical Allele Identifier: CA254038881
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1055037455
gnomAD v3: 13-84458011-G-A
gnomAD v4: 13-84458011-G-A
MyVariant Identifiers: chr13:g.85032146G>A (hg19) chr13:g.84458011G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458011G>A , CM000675.2:g.84458011G>A GRCh38
NC_000013.10:g.85032146G>A , CM000675.1:g.85032146G>A GRCh37
NC_000013.9:g.83930147G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104353G>A
XR_942133.1:n.369-46092C>T
XR_942134.1:n.366-46092C>T
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