Canonical Allele Identifier: CA741216150
Gene: LINC00687 HGNC NCBI

Linked Data

dbSNP Id: rs1285410276
gnomAD v3: 20-11810043-G-T
gnomAD v4: 20-11810043-G-T
MyVariant Identifiers: chr20:g.11790691G>T (hg19) chr20:g.11810043G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810043G>T , CM000682.2:g.11810043G>T GRCh38
NC_000020.10:g.11790691G>T , CM000682.1:g.11790691G>T GRCh37
NC_000020.9:g.11738691G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110635.1:n.468C>A
Search 100 bp 5'
Search 100 bp 3'