Canonical Allele Identifier: CA779420831

Gene: LINC00907

Linked Data

• dbSNP Id: rs1248105604
• gnomAD v3: 18-42470392-T-C
• gnomAD v4: 18-42470392-T-C
• MyVariant Identifiers: chr18:g.40050357T>C (hg19) ; chr18:g.42470392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42470392T>C , CM000680.2:g.42470392T>C	GRCh38
NC_000018.9:g.40050357T>C , CM000680.1:g.40050357T>C	GRCh37
NC_000018.8:g.38304355T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046174.2:n.872+15403T>C
NR_046454.1:n.652+15403T>C
NR_046455.1:n.489+15403T>C