Canonical Allele Identifier: CA824631127

Gene: LINC00951

Linked Data

• dbSNP Id: rs1234062776
• gnomAD v3: 6-40353962-C-G
• gnomAD v4: 6-40353962-C-G
• MyVariant Identifiers: chr6:g.40321701C>G (hg19) ; chr6:g.40353962C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353962C>G , CM000668.2:g.40353962C>G	GRCh38
NC_000006.11:g.40321701C>G , CM000668.1:g.40321701C>G	GRCh37
NC_000006.10:g.40429679C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2045G>C