Canonical Allele Identifier: CA1276001760
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680648640

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103961997C>A , CM000664.2:g.103961997C>A GRCh38
NC_000002.11:g.104578455C>A , CM000664.1:g.104578455C>A GRCh37
NC_000002.10:g.103944887C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87552C>A
XR_001739623.1:n.178+87552C>A