Canonical Allele Identifier: CA2782090155
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527709A>C , CM000670.2:g.125527709A>C GRCh38
NC_000008.10:g.126539951A>C , CM000670.1:g.126539951A>C GRCh37
NC_000008.9:g.126609133A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54395A>C
XR_001746072.1:n.583+4696A>C
XR_001746073.1:n.583+4696A>C