Canonical Allele Identifier: CA137815800

Gene: LINC00951

Linked Data

• dbSNP Id: rs753850399
• gnomAD v2: 6-40321828-C-T
• gnomAD v3: 6-40354089-C-T
• gnomAD v4: 6-40354089-C-T
• MyVariant Identifiers: chr6:g.40321828C>T (hg19) ; chr6:g.40354089C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354089C>T , CM000668.2:g.40354089C>T	GRCh38
NC_000006.11:g.40321828C>T , CM000668.1:g.40321828C>T	GRCh37
NC_000006.10:g.40429806C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1918G>A