Canonical Allele Identifier: CA254038886
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs534263640
gnomAD v3: 13-84458060-T-C
gnomAD v4: 13-84458060-T-C
MyVariant Identifiers: chr13:g.85032195T>C (hg19) chr13:g.84458060T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458060T>C , CM000675.2:g.84458060T>C GRCh38
NC_000013.10:g.85032195T>C , CM000675.1:g.85032195T>C GRCh37
NC_000013.9:g.83930196T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104304T>C
XR_942133.1:n.369-46141A>G
XR_942134.1:n.366-46141A>G
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