Canonical Allele Identifier: CA2840702488
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962032A>G , CM000664.2:g.103962032A>G GRCh38
NC_000002.11:g.104578490A>G , CM000664.1:g.104578490A>G GRCh37
NC_000002.10:g.103944922A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87587A>G
XR_001739623.1:n.178+87587A>G