Canonical Allele Identifier: CA1087445565
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763430422
gnomAD v3: 6-31306511-G-C
gnomAD v4: 6-31306511-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306511G>C , CM000668.2:g.31306511G>C GRCh38
NC_000006.11:g.31274288G>C , CM000668.1:g.31274288G>C GRCh37
NC_000006.10:g.31382267G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+267C>G
XR_926691.2:n.965+267C>G