Canonical Allele Identifier: CA1276001763
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680648740

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962002A>C , CM000664.2:g.103962002A>C GRCh38
NC_000002.11:g.104578460A>C , CM000664.1:g.104578460A>C GRCh37
NC_000002.10:g.103944892A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87557A>C
XR_001739623.1:n.178+87557A>C