Canonical Allele Identifier: CA943861425
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939611669
gnomAD v3: 11-134756877-C-T
gnomAD v4: 11-134756877-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756877C>T , CM000673.2:g.134756877C>T GRCh38
NC_000011.9:g.134626771C>T , CM000673.1:g.134626771C>T GRCh37
NC_000011.8:g.134131981C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147836.1:n.599-4197C>T
Search 100 bp 5'
Search 100 bp 3'