Canonical Allele Identifier: CA566857038

Gene: LINC00951

Linked Data

• dbSNP Id: rs1191529614
• gnomAD v2: 6-40321739-G-A
• gnomAD v3: 6-40354000-G-A
• gnomAD v4: 6-40354000-G-A
• MyVariant Identifiers: chr6:g.40321739G>A (hg19) ; chr6:g.40354000G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354000G>A , CM000668.2:g.40354000G>A	GRCh38
NC_000006.11:g.40321739G>A , CM000668.1:g.40321739G>A	GRCh37
NC_000006.10:g.40429717G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2007C>T