Canonical Allele Identifier: CA12175104

Gene: LINC03000

Linked Data

• dbSNP Id: rs10515889
• gnomAD v2: 5-164546897-A-G
• gnomAD v3: 5-165119891-A-G
• gnomAD v4: 5-165119891-A-G
• MyVariant Identifiers: chr5:g.164546897A>G (hg19) ; chr5:g.165119891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.165119891A>G , CM000667.2:g.165119891A>G	GRCh38
NC_000005.9:g.164546897A>G , CM000667.1:g.164546897A>G	GRCh37
NC_000005.8:g.164479475A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_941179.1:n.357-51487A>G