ClinGen Allele Registry
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Canonical Allele Identifier:
CA232144121
Gene: LINC02714
HGNC
NCBI
Linked Data
dbSNP Id:
rs78326128
gnomAD v2:
11-134626916-T-C
gnomAD v3:
11-134757022-T-C
gnomAD v4:
11-134757022-T-C
MyVariant Identifiers:
chr11:g.134626916T>C (hg19)
chr11:g.134757022T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.134757022T>C , CM000673.2:g.134757022T>C
GRCh38
NC_000011.9:g.134626916T>C , CM000673.1:g.134626916T>C
GRCh37
NC_000011.8:g.134132126T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_147836.1:n.599-4052T>C
Search 100 bp 5'
Search 100 bp 3'