Canonical Allele Identifier: CA2543196679
Gene: LINC02819 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484189T>C , CM000663.2:g.159484189T>C GRCh38
NC_000001.10:g.159453979T>C , CM000663.1:g.159453979T>C GRCh37
NC_000001.9:g.157720603T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1205T>C
XR_922189.3:n.690+1205T>C