Canonical Allele Identifier: CA14749991
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs62185668
gnomAD v2: 20-10961935-C-A
gnomAD v3: 20-10981287-C-A
gnomAD v4: 20-10981287-C-A
MyVariant Identifiers: chr20:g.10961935C>A (hg19) chr20:g.10981287C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10981287C>A , CM000682.2:g.10981287C>A GRCh38
NC_000020.10:g.10961935C>A , CM000682.1:g.10961935C>A GRCh37
NC_000020.9:g.10909935C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937255.1:n.3286-10311C>A
Search 100 bp 5'
Search 100 bp 3'