Canonical Allele Identifier: CA1817470552
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813380709

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527707T>C , CM000670.2:g.125527707T>C GRCh38
NC_000008.10:g.126539949T>C , CM000670.1:g.126539949T>C GRCh37
NC_000008.9:g.126609131T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54393T>C
XR_001746072.1:n.583+4694T>C
XR_001746073.1:n.583+4694T>C