Canonical Allele Identifier: CA11122033
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1036736

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962075T>C , CM000664.2:g.103962075T>C GRCh38
NC_000002.11:g.104578533T>C , CM000664.1:g.104578533T>C GRCh37
NC_000002.10:g.103944965T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87630T>C
XR_001739623.1:n.178+87630T>C