Canonical Allele Identifier: CA137815787

Gene: LINC00951

Linked Data

• dbSNP Id: rs973812684
• gnomAD v3: 6-40353964-T-A
• gnomAD v4: 6-40353964-T-A
• MyVariant Identifiers: chr6:g.40321703T>A (hg19) ; chr6:g.40353964T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353964T>A , CM000668.2:g.40353964T>A	GRCh38
NC_000006.11:g.40321703T>A , CM000668.1:g.40321703T>A	GRCh37
NC_000006.10:g.40429681T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2043A>T