Canonical Allele Identifier: CA1034488303
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1258873858

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962069C>T , CM000664.2:g.103962069C>T GRCh38
NC_000002.11:g.104578527C>T , CM000664.1:g.104578527C>T GRCh37
NC_000002.10:g.103944959C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87624C>T
XR_001739623.1:n.178+87624C>T