Canonical Allele Identifier: CA1619098707
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1472110876

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306682A>C , CM000668.2:g.31306682A>C GRCh38
NC_000006.11:g.31274459A>C , CM000668.1:g.31274459A>C GRCh37
NC_000006.10:g.31382438A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+96T>G
XR_926691.2:n.965+96T>G