Canonical Allele Identifier: CA1276001778
Gene: LINC01965 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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