Canonical Allele Identifier: CA262059637

Gene: LINC01500

Linked Data

• dbSNP Id: rs957202397
• gnomAD v3: 14-58867480-C-G
• gnomAD v4: 14-58867480-C-G
• MyVariant Identifiers: chr14:g.59334198C>G (hg19) ; chr14:g.58867480C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58867480C>G , CM000676.2:g.58867480C>G	GRCh38
NC_000014.8:g.59334198C>G , CM000676.1:g.59334198C>G	GRCh37
NC_000014.7:g.58403951C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110547.1:n.269-26663C>G