Canonical Allele Identifier: CA1817470560
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813381011

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527720A>C , CM000670.2:g.125527720A>C GRCh38
NC_000008.10:g.126539962A>C , CM000670.1:g.126539962A>C GRCh37
NC_000008.9:g.126609144A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54406A>C
XR_001746072.1:n.583+4707A>C
XR_001746073.1:n.583+4707A>C