Canonical Allele Identifier: CA566857047

Gene: LINC00951

Linked Data

• dbSNP Id: rs1157168649
• gnomAD v2: 6-40321838-A-G
• gnomAD v3: 6-40354099-A-G
• gnomAD v4: 6-40354099-A-G
• MyVariant Identifiers: chr6:g.40321838A>G (hg19) ; chr6:g.40354099A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354099A>G , CM000668.2:g.40354099A>G	GRCh38
NC_000006.11:g.40321838A>G , CM000668.1:g.40321838A>G	GRCh37
NC_000006.10:g.40429816A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1908T>C