Canonical Allele Identifier: CA958336048
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879683577
gnomAD v3: 13-84458172-T-G
gnomAD v4: 13-84458172-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458172T>G , CM000675.2:g.84458172T>G GRCh38
NC_000013.10:g.85032307T>G , CM000675.1:g.85032307T>G GRCh37
NC_000013.9:g.83930308T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104192T>G
XR_942133.1:n.369-46253A>C
XR_942134.1:n.366-46253A>C
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