Canonical Allele Identifier: CA53064898
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs766157299
MyVariant Identifiers: chr2:g.104578522C>G (hg19) chr2:g.103962064C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962064C>G , CM000664.2:g.103962064C>G GRCh38
NC_000002.11:g.104578522C>G , CM000664.1:g.104578522C>G GRCh37
NC_000002.10:g.103944954C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87619C>G
XR_001739623.1:n.178+87619C>G
Search 100 bp 5'
Search 100 bp 3'