Canonical Allele Identifier: CA824631258

Gene: LINC00951

Linked Data

• dbSNP Id: rs1474644361
• MyVariant Identifiers: chr6:g.40321896_40321898del (hg19) ; chr6:g.40354157_40354159del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354163_40354165del , CM000668.2:g.40354163_40354165del	GRCh38
NC_000006.11:g.40321902_40321904del , CM000668.1:g.40321902_40321904del	GRCh37
NC_000006.10:g.40429880_40429882del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1848_1850del