Canonical Allele Identifier: CA136833266
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs9264936
gnomAD v2: 6-31274257-G-C
gnomAD v3: 6-31306480-G-C
gnomAD v4: 6-31306480-G-C
MyVariant Identifiers: chr6:g.31274257G>C (hg19) chr6:g.31306480G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306480G>C , CM000668.2:g.31306480G>C GRCh38
NC_000006.11:g.31274257G>C , CM000668.1:g.31274257G>C GRCh37
NC_000006.10:g.31382236G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+298C>G
XR_926691.2:n.965+298C>G
Search 100 bp 5'
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