Canonical Allele Identifier: CA754459801
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1475042494

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962047C>A , CM000664.2:g.103962047C>A GRCh38
NC_000002.11:g.104578505C>A , CM000664.1:g.104578505C>A GRCh37
NC_000002.10:g.103944937C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87602C>A
XR_001739623.1:n.178+87602C>A