Canonical Allele Identifier: CA53064922
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1010614854

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962191G>A , CM000664.2:g.103962191G>A GRCh38
NC_000002.11:g.104578649G>A , CM000664.1:g.104578649G>A GRCh37
NC_000002.10:g.103945081G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87746G>A
XR_001739623.1:n.178+87746G>A