Canonical Allele Identifier: CA137815809

Gene: LINC00951

Linked Data

• dbSNP Id: rs1003846399
• gnomAD v2: 6-40321959-G-A
• gnomAD v3: 6-40354220-G-A
• gnomAD v4: 6-40354220-G-A
• MyVariant Identifiers: chr6:g.40321959G>A (hg19) ; chr6:g.40354220G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354220G>A , CM000668.2:g.40354220G>A	GRCh38
NC_000006.11:g.40321959G>A , CM000668.1:g.40321959G>A	GRCh37
NC_000006.10:g.40429937G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1787C>T