Canonical Allele Identifier: CA1087445592
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1763439326
gnomAD v3: 6-31306658-A-G
gnomAD v4: 6-31306658-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306658A>G , CM000668.2:g.31306658A>G GRCh38
NC_000006.11:g.31274435A>G , CM000668.1:g.31274435A>G GRCh37
NC_000006.10:g.31382414A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+120T>C
XR_926691.2:n.965+120T>C