Canonical Allele Identifier: CA634619985
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs1295473886
gnomAD v2: 20-10850412-T-C
gnomAD v3: 20-10869764-T-C
gnomAD v4: 20-10869764-T-C
MyVariant Identifiers: chr20:g.10850412T>C (hg19) chr20:g.10869764T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869764T>C , CM000682.2:g.10869764T>C GRCh38
NC_000020.10:g.10850412T>C , CM000682.1:g.10850412T>C GRCh37
NC_000020.9:g.10798412T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2457T>C
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