Canonical Allele Identifier: CA774555020
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1357197361
MyVariant Identifiers: chr17:g.67850937A>G (hg19) chr17:g.69854796A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854796A>G , CM000679.2:g.69854796A>G GRCh38
NC_000017.10:g.67850937A>G , CM000679.1:g.67850937A>G GRCh37
NC_000017.9:g.65362532A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9310A>G
NR_109972.1:n.363+9310A>G
Search 100 bp 5'
Search 100 bp 3'