Canonical Allele Identifier: CA53064885
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs372096484

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962029T>C , CM000664.2:g.103962029T>C GRCh38
NC_000002.11:g.104578487T>C , CM000664.1:g.104578487T>C GRCh37
NC_000002.10:g.103944919T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87584T>C
XR_001739623.1:n.178+87584T>C