Canonical Allele Identifier: CA2718229911
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs2129945376

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527778C>G , CM000670.2:g.125527778C>G GRCh38
NC_000008.10:g.126540020C>G , CM000670.1:g.126540020C>G GRCh37
NC_000008.9:g.126609202C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54464C>G
XR_001746072.1:n.583+4765C>G
XR_001746073.1:n.583+4765C>G