Canonical Allele Identifier: CA741127738
Gene: LINC02871 HGNC NCBI

Linked Data

dbSNP Id: rs1356166339
MyVariant Identifiers: chr20:g.10850373A>G (hg19) chr20:g.10869725A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869725A>G , CM000682.2:g.10869725A>G GRCh38
NC_000020.10:g.10850373A>G , CM000682.1:g.10850373A>G GRCh37
NC_000020.9:g.10798373A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937255.1:n.2829+2418A>G
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