Canonical Allele Identifier: CA1817470573
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813381593

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527763T>G , CM000670.2:g.125527763T>G GRCh38
NC_000008.10:g.126540005T>G , CM000670.1:g.126540005T>G GRCh37
NC_000008.9:g.126609187T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54449T>G
XR_001746072.1:n.583+4750T>G
XR_001746073.1:n.583+4750T>G