Canonical Allele Identifier: CA1619098680
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763439157

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306655T>G , CM000668.2:g.31306655T>G GRCh38
NC_000006.11:g.31274432T>G , CM000668.1:g.31274432T>G GRCh37
NC_000006.10:g.31382411T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+123A>C
XR_926691.2:n.965+123A>C