Canonical Allele Identifier: CA1276001866
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680652705
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962218C>A , CM000664.2:g.103962218C>A GRCh38
NC_000002.11:g.104578676C>A , CM000664.1:g.104578676C>A GRCh37
NC_000002.10:g.103945108C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87773C>A
XR_001739623.1:n.178+87773C>A
Search 100 bp 5'
Search 100 bp 3'