Canonical Allele Identifier: CA14452924
Gene: LINC01483 HGNC NCBI
dbSNP:
11870477
gnomAD v2:
17:67802352 A / C
gnomAD v3:
17:69806211 A / C
gnomAD v4:
chr17-69806211-A-C
Joint Max Group AF 0.28248893 (EAS)
Genomes Max Group AF 0.28248893 (EAS)
MyVariant.info:
GRCh38 chr17:g.69806211A>C
GRCh37 chr17:g.67802352A>C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69806211A>C , CM000679.2:g.69806211A>C GRCh38
NC_000017.10:g.67802352A>C , CM000679.1:g.67802352A>C GRCh37
NC_000017.9:g.65313947A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.317-39229A>C
NR_109972.1:n.317-39229A>C
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