ClinGen Allele Registry
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Canonical Allele Identifier:
CA232144119
Gene: LINC02714
HGNC
NCBI
Linked Data
dbSNP Id:
rs1018701152
gnomAD v2:
11-134626913-G-T
gnomAD v3:
11-134757019-G-T
gnomAD v4:
11-134757019-G-T
MyVariant Identifiers:
chr11:g.134626913G>T (hg19)
chr11:g.134757019G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.134757019G>T , CM000673.2:g.134757019G>T
GRCh38
NC_000011.9:g.134626913G>T , CM000673.1:g.134626913G>T
GRCh37
NC_000011.8:g.134132123G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_147836.1:n.599-4055G>T
Search 100 bp 5'
Search 100 bp 3'