Canonical Allele Identifier: CA1817470612
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813383140

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527834A>G , CM000670.2:g.125527834A>G GRCh38
NC_000008.10:g.126540076A>G , CM000670.1:g.126540076A>G GRCh37
NC_000008.9:g.126609258A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54520A>G
XR_001746072.1:n.583+4821A>G
XR_001746073.1:n.583+4821A>G