ClinGen Allele Registry
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Canonical Allele Identifier:
CA725329732
Gene: FENDRR
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.86478309T>A
GRCh37
chr16:g.86511915T>A
Linked Data - NCBI & NCI
dbSNP:
7187365
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.86478309T>A , CM000678.2:g.86478309T>A
GRCh38
NC_000016.9:g.86511915T>A , CM000678.1:g.86511915T>A
GRCh37
NC_000016.8:g.85069416T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033925.1:n.259-258A>T
Search 100 bp 5'
Search 100 bp 3'