Canonical Allele Identifier: CA1619098657
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763437458

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306612T>C , CM000668.2:g.31306612T>C GRCh38
NC_000006.11:g.31274389T>C , CM000668.1:g.31274389T>C GRCh37
NC_000006.10:g.31382368T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+166A>G
XR_926691.2:n.965+166A>G