Canonical Allele Identifier: CA1623081745
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762014970

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354123dup , CM000668.2:g.40354123dup GRCh38
NC_000006.11:g.40321862dup , CM000668.1:g.40321862dup GRCh37
NC_000006.10:g.40429840dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1884dup