Canonical Allele Identifier: CA293666677
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs368727820
gnomAD v2: 17-67851014-G-A
gnomAD v3: 17-69854873-G-A
gnomAD v4: 17-69854873-G-A
MyVariant Identifiers: chr17:g.67851014G>A (hg19) chr17:g.69854873G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854873G>A , CM000679.2:g.69854873G>A GRCh38
NC_000017.10:g.67851014G>A , CM000679.1:g.67851014G>A GRCh37
NC_000017.9:g.65362609G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9387G>A
NR_109972.1:n.363+9387G>A
Search 100 bp 5'
Search 100 bp 3'