Canonical Allele Identifier: CA824631123

Gene: LINC00951

Linked Data

• dbSNP Id: rs1348884567
• gnomAD v3: 6-40353954-C-T
• gnomAD v4: 6-40353954-C-T
• MyVariant Identifiers: chr6:g.40321693C>T (hg19) ; chr6:g.40353954C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353954C>T , CM000668.2:g.40353954C>T	GRCh38
NC_000006.11:g.40321693C>T , CM000668.1:g.40321693C>T	GRCh37
NC_000006.10:g.40429671C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2053G>A