Canonical Allele Identifier: CA566857051

Gene: LINC00951

Linked Data

• dbSNP Id: rs1302958524
• gnomAD v2: 6-40321866-C-G
• gnomAD v3: 6-40354127-C-G
• gnomAD v4: 6-40354127-C-G
• MyVariant Identifiers: chr6:g.40321866C>G (hg19) ; chr6:g.40354127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354127C>G , CM000668.2:g.40354127C>G	GRCh38
NC_000006.11:g.40321866C>G , CM000668.1:g.40321866C>G	GRCh37
NC_000006.10:g.40429844C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1880G>C