Canonical Allele Identifier: CA566857033

Gene: LINC00951

Linked Data

• dbSNP Id: rs1242137022
• gnomAD v2: 6-40321707-G-A
• gnomAD v3: 6-40353968-G-A
• gnomAD v4: 6-40353968-G-A
• MyVariant Identifiers: chr6:g.40321707G>A (hg19) ; chr6:g.40353968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353968G>A , CM000668.2:g.40353968G>A	GRCh38
NC_000006.11:g.40321707G>A , CM000668.1:g.40321707G>A	GRCh37
NC_000006.10:g.40429685G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2039C>T