Canonical Allele Identifier: CA823866995

Gene: LINC02571

Linked Data

• dbSNP Id: rs1161626846
• gnomAD v3: 6-31306506-G-A
• gnomAD v4: 6-31306506-G-A
• MyVariant Identifiers: chr6:g.31274283G>A (hg19) ; chr6:g.31306506G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306506G>A , CM000668.2:g.31306506G>A	GRCh38
NC_000006.11:g.31274283G>A , CM000668.1:g.31274283G>A	GRCh37
NC_000006.10:g.31382262G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+272C>T
XR_926691.2:n.965+272C>T