Canonical Allele Identifier: CA566338531
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1472110876
gnomAD v2: 6-31274459-A-G
gnomAD v3: 6-31306682-A-G
gnomAD v4: 6-31306682-A-G
MyVariant Identifiers: chr6:g.31274459A>G (hg19) chr6:g.31306682A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306682A>G , CM000668.2:g.31306682A>G GRCh38
NC_000006.11:g.31274459A>G , CM000668.1:g.31274459A>G GRCh37
NC_000006.10:g.31382438A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+96T>C
XR_926691.2:n.965+96T>C
Search 100 bp 5'
Search 100 bp 3'