Canonical Allele Identifier: CA1201917070
Gene: LINC02819 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484238A= , CM000663.2:g.159484238A= GRCh38
NC_000001.10:g.159454028A= , CM000663.1:g.159454028A= GRCh37
NC_000001.9:g.157720652A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1254A=
XR_922189.3:n.690+1254A=