Canonical Allele Identifier: CA2532967820
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962049T>G , CM000664.2:g.103962049T>G GRCh38
NC_000002.11:g.104578507T>G , CM000664.1:g.104578507T>G GRCh37
NC_000002.10:g.103944939T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87604T>G
XR_001739623.1:n.178+87604T>G