Canonical Allele Identifier: CA854344912
Gene: LINC01299 HGNC NCBI

Linked Data

dbSNP Id: rs6981992
MyVariant Identifiers: chr8:g.66463478G>A (hg19) chr8:g.65551243G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.65551243G>A , CM000670.2:g.65551243G>A GRCh38
NC_000008.10:g.66463478G>A , CM000670.1:g.66463478G>A GRCh37
NC_000008.9:g.66626032G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033893.1:n.61+11363C>T
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