Canonical Allele Identifier: CA137815806

Gene: LINC00951

Linked Data

• dbSNP Id: rs117230261
• gnomAD v2: 6-40321912-A-T
• gnomAD v3: 6-40354173-A-T
• gnomAD v4: 6-40354173-A-T
• MyVariant Identifiers: chr6:g.40321912A>T (hg19) ; chr6:g.40354173A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354173A>T , CM000668.2:g.40354173A>T	GRCh38
NC_000006.11:g.40321912A>T , CM000668.1:g.40321912A>T	GRCh37
NC_000006.10:g.40429890A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1834T>A