Canonical Allele Identifier: CA779420906

Gene: LINC00907

Linked Data

• dbSNP Id: rs1409761083
• gnomAD v3: 18-42470497-C-T
• gnomAD v4: 18-42470497-C-T
• MyVariant Identifiers: chr18:g.40050462C>T (hg19) ; chr18:g.42470497C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42470497C>T , CM000680.2:g.42470497C>T	GRCh38
NC_000018.9:g.40050462C>T , CM000680.1:g.40050462C>T	GRCh37
NC_000018.8:g.38304460C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.872+15508C>T
NR_046454.1:n.652+15508C>T
NR_046455.1:n.489+15508C>T