Canonical Allele Identifier: CA2565853170
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962036G>C , CM000664.2:g.103962036G>C GRCh38
NC_000002.11:g.104578494G>C , CM000664.1:g.104578494G>C GRCh37
NC_000002.10:g.103944926G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87591G>C
XR_001739623.1:n.178+87591G>C