Canonical Allele Identifier: CA566857053

Gene: LINC00951

Linked Data

• dbSNP Id: rs1393997660
• gnomAD v2: 6-40321900-G-T
• gnomAD v3: 6-40354161-G-T
• gnomAD v4: 6-40354161-G-T
• MyVariant Identifiers: chr6:g.40321900G>T (hg19) ; chr6:g.40354161G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354161G>T , CM000668.2:g.40354161G>T	GRCh38
NC_000006.11:g.40321900G>T , CM000668.1:g.40321900G>T	GRCh37
NC_000006.10:g.40429878G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1846C>A