Canonical Allele Identifier: CA1276001781
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680649400

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962042G>A , CM000664.2:g.103962042G>A GRCh38
NC_000002.11:g.104578500G>A , CM000664.1:g.104578500G>A GRCh37
NC_000002.10:g.103944932G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87597G>A
XR_001739623.1:n.178+87597G>A