Canonical Allele Identifier: CA293666678
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs368727820
gnomAD v2: 17-67851014-G-T
gnomAD v3: 17-69854873-G-T
gnomAD v4: 17-69854873-G-T
MyVariant Identifiers: chr17:g.67851014G>T (hg19) chr17:g.69854873G>T (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9387G>T
NR_109972.1:n.363+9387G>T
Search 100 bp 5'
Search 100 bp 3'