Canonical Allele Identifier: CA232144134
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs190230949
gnomAD v2: 11-134627019-G-T
gnomAD v3: 11-134757125-G-T
gnomAD v4: 11-134757125-G-T
MyVariant Identifiers: chr11:g.134627019G>T (hg19) chr11:g.134757125G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134757125G>T , CM000673.2:g.134757125G>T GRCh38
NC_000011.9:g.134627019G>T , CM000673.1:g.134627019G>T GRCh37
NC_000011.8:g.134132229G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-3949G>T
Search 100 bp 5'
Search 100 bp 3'