Canonical Allele Identifier: CA741127750
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs1235073098
MyVariant Identifiers: chr20:g.10850427C>T (hg19) chr20:g.10869779C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869779C>T , CM000682.2:g.10869779C>T GRCh38
NC_000020.10:g.10850427C>T , CM000682.1:g.10850427C>T GRCh37
NC_000020.9:g.10798427C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2472C>T
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