ClinGen Allele Registry
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Canonical Allele Identifier:
CA311933743
Gene: LINC00687
HGNC
NCBI
Linked Data
dbSNP Id:
rs1136200
gnomAD v2:
20-11790686-G-T
gnomAD v3:
20-11810038-G-T
gnomAD v4:
20-11810038-G-T
MyVariant Identifiers:
chr20:g.11790686G>T (hg19)
chr20:g.11810038G>T (hg38)
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'