Canonical Allele Identifier: CA611350510
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1312189575
gnomAD v2: 13-85032176-A-G
gnomAD v3: 13-84458041-A-G
gnomAD v4: 13-84458041-A-G
MyVariant Identifiers: chr13:g.85032176A>G (hg19) chr13:g.84458041A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458041A>G , CM000675.2:g.84458041A>G GRCh38
NC_000013.10:g.85032176A>G , CM000675.1:g.85032176A>G GRCh37
NC_000013.9:g.83930177A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104323A>G
XR_942133.1:n.369-46122T>C
XR_942134.1:n.366-46122T>C
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