Canonical Allele Identifier: CA1276001828
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680651577

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962136A>G , CM000664.2:g.103962136A>G GRCh38
NC_000002.11:g.104578594A>G , CM000664.1:g.104578594A>G GRCh37
NC_000002.10:g.103945026A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87691A>G
XR_001739623.1:n.178+87691A>G