Canonical Allele Identifier: CA1817470587
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs72645161

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527803G>C , CM000670.2:g.125527803G>C GRCh38
NC_000008.10:g.126540045G>C , CM000670.1:g.126540045G>C GRCh37
NC_000008.9:g.126609227G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54489G>C
XR_001746072.1:n.583+4790G>C
XR_001746073.1:n.583+4790G>C