Canonical Allele Identifier: CA1619098568
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763429444
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306501T>A , CM000668.2:g.31306501T>A GRCh38
NC_000006.11:g.31274278T>A , CM000668.1:g.31274278T>A GRCh37
NC_000006.10:g.31382257T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+277A>T
XR_926691.2:n.965+277A>T
Search 100 bp 5'
Search 100 bp 3'