Canonical Allele Identifier: CA1087445577
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763435477
gnomAD v3: 6-31306588-G-A
gnomAD v4: 6-31306588-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306588G>A , CM000668.2:g.31306588G>A GRCh38
NC_000006.11:g.31274365G>A , CM000668.1:g.31274365G>A GRCh37
NC_000006.10:g.31382344G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+190C>T
XR_926691.2:n.965+190C>T