Canonical Allele Identifier: CA53064913
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs922810145
MyVariant Identifiers: chr2:g.103962143C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962143C>T , CM000664.2:g.103962143C>T GRCh38
NC_000002.11:g.104578601C>T , CM000664.1:g.104578601C>T GRCh37
NC_000002.10:g.103945033C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87698C>T
XR_001739623.1:n.178+87698C>T