Canonical Allele Identifier: CA1619098665
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763437977

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306627C>T , CM000668.2:g.31306627C>T GRCh38
NC_000006.11:g.31274404C>T , CM000668.1:g.31274404C>T GRCh37
NC_000006.10:g.31382383C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+151G>A
XR_926691.2:n.965+151G>A