Canonical Allele Identifier: CA3085520663
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103956547C>G , CM000664.2:g.103956547C>G GRCh38
NC_000002.11:g.104573005C>G , CM000664.1:g.104573005C>G GRCh37
NC_000002.10:g.103939437C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+82102C>G
XR_001739623.1:n.178+82102C>G