Canonical Allele Identifier: CA890035979
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1371477939
MyVariant Identifiers: chr1:g.159453960G>A (hg19) chr1:g.159484170G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484170G>A , CM000663.2:g.159484170G>A GRCh38
NC_000001.10:g.159453960G>A , CM000663.1:g.159453960G>A GRCh37
NC_000001.9:g.157720584G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1186G>A
XR_922189.3:n.690+1186G>A
Search 100 bp 5'
Search 100 bp 3'