Canonical Allele Identifier: CA774554998
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1184096801
gnomAD v3: 17-69854645-T-C
gnomAD v4: 17-69854645-T-C
MyVariant Identifiers: chr17:g.67850786T>C (hg19) chr17:g.69854645T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854645T>C , CM000679.2:g.69854645T>C GRCh38
NC_000017.10:g.67850786T>C , CM000679.1:g.67850786T>C GRCh37
NC_000017.9:g.65362381T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9159T>C
NR_109972.1:n.363+9159T>C
Search 100 bp 5'
Search 100 bp 3'