Canonical Allele Identifier: CA12367933
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs6931332
gnomAD v2: 6-31274245-A-G
gnomAD v3: 6-31306468-A-G
gnomAD v4: 6-31306468-A-G
MyVariant Identifiers: chr6:g.31274245A>G (hg19) chr6:g.31306468A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306468A>G , CM000668.2:g.31306468A>G GRCh38
NC_000006.11:g.31274245A>G , CM000668.1:g.31274245A>G GRCh37
NC_000006.10:g.31382224A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+310T>C
XR_926691.2:n.965+310T>C
Search 100 bp 5'
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