Canonical Allele Identifier: CA1088161023
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762014757

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354112del , CM000668.2:g.40354112del GRCh38
NC_000006.11:g.40321851del , CM000668.1:g.40321851del GRCh37
NC_000006.10:g.40429829del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1898del