Canonical Allele Identifier: CA185516675
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1025796638

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527844A>G , CM000670.2:g.125527844A>G GRCh38
NC_000008.10:g.126540086A>G , CM000670.1:g.126540086A>G GRCh37
NC_000008.9:g.126609268A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54530A>G
XR_001746072.1:n.583+4831A>G
XR_001746073.1:n.583+4831A>G