Canonical Allele Identifier: CA2727180371
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs2135521890

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398920G>C , CM000674.2:g.111398920G>C GRCh38
NC_000012.11:g.111836724G>C , CM000674.1:g.111836724G>C GRCh37
NC_000012.10:g.110321107G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2047G>C