Canonical Allele Identifier: CA2711319395
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2113771095

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354222_40354226del , CM000668.2:g.40354222_40354226del GRCh38
NC_000006.11:g.40321961_40321965del , CM000668.1:g.40321961_40321965del GRCh37
NC_000006.10:g.40429939_40429943del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1782_1786del