Canonical Allele Identifier: CA53064886
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs960370275

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962037C>T , CM000664.2:g.103962037C>T GRCh38
NC_000002.11:g.104578495C>T , CM000664.1:g.104578495C>T GRCh37
NC_000002.10:g.103944927C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87592C>T
XR_001739623.1:n.178+87592C>T