Canonical Allele Identifier: CA136833272
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs9264938
gnomAD v2: 6-31274269-T-A
gnomAD v3: 6-31306492-T-A
gnomAD v4: 6-31306492-T-A
MyVariant Identifiers: chr6:g.31274269T>A (hg19) chr6:g.31306492T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306492T>A , CM000668.2:g.31306492T>A GRCh38
NC_000006.11:g.31274269T>A , CM000668.1:g.31274269T>A GRCh37
NC_000006.10:g.31382248T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926691.1:n.949+286A>T
XR_926691.2:n.965+286A>T
Search 100 bp 5'
Search 100 bp 3'