Canonical Allele Identifier: CA137815812

Gene: LINC00951

Linked Data

• dbSNP Id: rs550683783
• gnomAD v3: 6-40354240-C-T
• gnomAD v4: 6-40354240-C-T
• MyVariant Identifiers: chr6:g.40321979C>T (hg19) ; chr6:g.40354240C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354240C>T , CM000668.2:g.40354240C>T	GRCh38
NC_000006.11:g.40321979C>T , CM000668.1:g.40321979C>T	GRCh37
NC_000006.10:g.40429957C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1767G>A