Canonical Allele Identifier: CA917711190
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1582412598

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306504_31306505insTTTGA , CM000668.2:g.31306504_31306505insTTTGA GRCh38
NC_000006.11:g.31274281_31274282insTTTGA , CM000668.1:g.31274281_31274282insTTTGA GRCh37
NC_000006.10:g.31382260_31382261insTTTGA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+273_949+274insTCAAA
XR_926691.2:n.965+273_965+274insTCAAA