Canonical Allele Identifier: CA31223081
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs4133289

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484147C>T , CM000663.2:g.159484147C>T GRCh38
NC_000001.10:g.159453937C>T , CM000663.1:g.159453937C>T GRCh37
NC_000001.9:g.157720561C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922189.1:n.678+1163C>T
XR_922189.3:n.690+1163C>T