Canonical Allele Identifier: CA1008293319
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1656898197
gnomAD v3: 1-159484174-C-G
gnomAD v4: 1-159484174-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484174C>G , CM000663.2:g.159484174C>G GRCh38
NC_000001.10:g.159453964C>G , CM000663.1:g.159453964C>G GRCh37
NC_000001.9:g.157720588C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1190C>G
XR_922189.3:n.690+1190C>G
Search 100 bp 5'
Search 100 bp 3'