Canonical Allele Identifier: CA185516669
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1040005767

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527822C>T , CM000670.2:g.125527822C>T GRCh38
NC_000008.10:g.126540064C>T , CM000670.1:g.126540064C>T GRCh37
NC_000008.9:g.126609246C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54508C>T
XR_001746072.1:n.583+4809C>T
XR_001746073.1:n.583+4809C>T