Canonical Allele Identifier: CA1008293249

Gene: LINC02819

Linked Data

• dbSNP Id: rs957559061
• gnomAD v3: 1-159484067-C-T
• gnomAD v4: 1-159484067-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484067C>T , CM000663.2:g.159484067C>T	GRCh38
NC_000001.10:g.159453857C>T , CM000663.1:g.159453857C>T	GRCh37
NC_000001.9:g.157720481C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1083C>T
XR_922189.3:n.690+1083C>T