Canonical Allele Identifier: CA823866999

Gene: LINC02571

Linked Data

• dbSNP Id: rs1240761959
• gnomAD v3: 6-31306572-T-C
• gnomAD v4: 6-31306572-T-C
• MyVariant Identifiers: chr6:g.31274349T>C (hg19) ; chr6:g.31306572T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31306572T>C , CM000668.2:g.31306572T>C	GRCh38
NC_000006.11:g.31274349T>C , CM000668.1:g.31274349T>C	GRCh37
NC_000006.10:g.31382328T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926691.1:n.949+206A>G
XR_926691.2:n.965+206A>G