Canonical Allele Identifier: CA137815789

Gene: LINC00951

Linked Data

• dbSNP Id: rs751719393
• gnomAD v2: 6-40321705-G-A
• gnomAD v3: 6-40353966-G-A
• gnomAD v4: 6-40353966-G-A
• MyVariant Identifiers: chr6:g.40321705G>A (hg19) ; chr6:g.40353966G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353966G>A , CM000668.2:g.40353966G>A	GRCh38
NC_000006.11:g.40321705G>A , CM000668.1:g.40321705G>A	GRCh37
NC_000006.10:g.40429683G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.2041C>T