Canonical Allele Identifier: CA951840640
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1871267962

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399088T>C , CM000674.2:g.111399088T>C GRCh38
NC_000012.11:g.111836892T>C , CM000674.1:g.111836892T>C GRCh37
NC_000012.10:g.110321275T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2215T>C