Canonical Allele Identifier: CA1619098627
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763435789
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306594C>A , CM000668.2:g.31306594C>A GRCh38
NC_000006.11:g.31274371C>A , CM000668.1:g.31274371C>A GRCh37
NC_000006.10:g.31382350C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+184G>T
XR_926691.2:n.965+184G>T
Search 100 bp 5'
Search 100 bp 3'