Canonical Allele Identifier: CA137815797

Gene: LINC00951

Linked Data

• dbSNP Id: rs894283561
• gnomAD v3: 6-40354078-T-C
• gnomAD v4: 6-40354078-T-C
• MyVariant Identifiers: chr6:g.40321817T>C (hg19) ; chr6:g.40354078T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354078T>C , CM000668.2:g.40354078T>C	GRCh38
NC_000006.11:g.40321817T>C , CM000668.1:g.40321817T>C	GRCh37
NC_000006.10:g.40429795T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1929A>G