Canonical Allele Identifier: CA254056592
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs2197609
gnomAD v2: 13-85177888-T-G
gnomAD v3: 13-84603753-T-G
gnomAD v4: 13-84603753-T-G
MyVariant Identifiers: chr13:g.85177888T>G (hg19) chr13:g.84603753T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84603753T>G , CM000675.2:g.84603753T>G GRCh38
NC_000013.10:g.85177888T>G , CM000675.1:g.85177888T>G GRCh37
NC_000013.9:g.84075889T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.750-2953T>G
XR_942132.1:n.103-2104A>C
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