Canonical Allele Identifier: CA1817470640
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813383997

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527878C>G , CM000670.2:g.125527878C>G GRCh38
NC_000008.10:g.126540120C>G , CM000670.1:g.126540120C>G GRCh37
NC_000008.9:g.126609302C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54564C>G
XR_001746072.1:n.583+4865C>G
XR_001746073.1:n.583+4865C>G