Canonical Allele Identifier: CA566857046

Gene: LINC00951

Linked Data

• dbSNP Id: rs1421908858
• gnomAD v2: 6-40321837-T-TG
• gnomAD v3: 6-40354098-T-TG
• gnomAD v4: 6-40354098-T-TG
• MyVariant Identifiers: chr6:g.40321837_40321838insG (hg19) ; chr6:g.40354098_40354099insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354098_40354099insG , CM000668.2:g.40354098_40354099insG	GRCh38
NC_000006.11:g.40321837_40321838insG , CM000668.1:g.40321837_40321838insG	GRCh37
NC_000006.10:g.40429815_40429816insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1908_1909insC