Canonical Allele Identifier: CA824631179
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1243184517

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354029_40354031del , CM000668.2:g.40354029_40354031del GRCh38
NC_000006.11:g.40321768_40321770del , CM000668.1:g.40321768_40321770del GRCh37
NC_000006.10:g.40429746_40429748del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1978_1980del