Canonical Allele Identifier: CA1015455257
Gene: LINC00687 HGNC NCBI

Linked Data

dbSNP Id: rs2056408609
gnomAD v3: 20-11810041-C-A
gnomAD v4: 20-11810041-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810041C>A , CM000682.2:g.11810041C>A GRCh38
NC_000020.10:g.11790689C>A , CM000682.1:g.11790689C>A GRCh37
NC_000020.9:g.11738689C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110635.1:n.470G>T
Search 100 bp 5'
Search 100 bp 3'