Canonical Allele Identifier: CA1619098594
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1735696922

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306530_31306531insAAAA , CM000668.2:g.31306530_31306531insAAAA GRCh38
NC_000006.11:g.31274307_31274308insAAAA , CM000668.1:g.31274307_31274308insAAAA GRCh37
NC_000006.10:g.31382286_31382287insAAAA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+247_949+248insTTTT
XR_926691.2:n.965+247_965+248insTTTT