Canonical Allele Identifier: CA137815790

Gene: LINC00951

Linked Data

• dbSNP Id: rs577648782
• gnomAD v3: 6-40354017-A-G
• gnomAD v4: 6-40354017-A-G
• MyVariant Identifiers: chr6:g.40321756A>G (hg19) ; chr6:g.40354017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354017A>G , CM000668.2:g.40354017A>G	GRCh38
NC_000006.11:g.40321756A>G , CM000668.1:g.40321756A>G	GRCh37
NC_000006.10:g.40429734A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1990T>C