Canonical Allele Identifier: CA566338523
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs1455514311
gnomAD v2: 6-31274253-C-A
gnomAD v3: 6-31306476-C-A
gnomAD v4: 6-31306476-C-A
MyVariant Identifiers: chr6:g.31274253C>A (hg19) chr6:g.31306476C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306476C>A , CM000668.2:g.31306476C>A GRCh38
NC_000006.11:g.31274253C>A , CM000668.1:g.31274253C>A GRCh37
NC_000006.10:g.31382232C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+302G>T
XR_926691.2:n.965+302G>T
Search 100 bp 5'
Search 100 bp 3'