Canonical Allele Identifier: CA311933743
Gene: LINC00687 HGNC NCBI
MyVariant.info:
GRCh38 chr20:g.11810038G>T
GRCh37 chr20:g.11790686G>T
gnomAD v2:
20:11790686 G / T
gnomAD v3:
20:11810038 G / T
gnomAD v4:
chr20-11810038-G-T
Joint Max Group AF 0.03863202 (EAS)
Genomes Max Group AF 0.03863202 (EAS)
Exomes Max Group AF 0.00185072 (NFE)
dbSNP:
1136200
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.11810038G>T , CM000682.2:g.11810038G>T GRCh38
NC_000020.10:g.11790686G>T , CM000682.1:g.11790686G>T GRCh37
NC_000020.9:g.11738686G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110635.1:n.473C>A
Search 100 bp 5'
Search 100 bp 3'