Canonical Allele Identifier: CA566857035

Gene: LINC00951

Linked Data

• dbSNP Id: rs1290842284
• gnomAD v2: 6-40321716-TG-T
• gnomAD v3: 6-40353977-TG-T
• gnomAD v4: 6-40353977-TG-T
• MyVariant Identifiers: chr6:g.40321717del (hg19) ; chr6:g.40353978del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353978del , CM000668.2:g.40353978del	GRCh38
NC_000006.11:g.40321717del , CM000668.1:g.40321717del	GRCh37
NC_000006.10:g.40429695del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2029del