Canonical Allele Identifier: CA11158052
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103970893T>A , CM000664.2:g.103970893T>A GRCh38
NC_000002.11:g.104587351T>A , CM000664.1:g.104587351T>A GRCh37
NC_000002.10:g.103953783T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.179-82611T>A
XR_001739623.1:n.179-82611T>A