Canonical Allele Identifier: CA1276002801
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs12613775

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103964045C>G , CM000664.2:g.103964045C>G GRCh38
NC_000002.11:g.104580503C>G , CM000664.1:g.104580503C>G GRCh37
NC_000002.10:g.103946935C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.179-89459C>G
XR_001739623.1:n.179-89459C>G