Canonical Allele Identifier: CA53064891
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs905771098

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962041A>G , CM000664.2:g.103962041A>G GRCh38
NC_000002.11:g.104578499A>G , CM000664.1:g.104578499A>G GRCh37
NC_000002.10:g.103944931A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87596A>G
XR_001739623.1:n.178+87596A>G