Canonical Allele Identifier: CA779420766
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1197657147
gnomAD v3: 18-42470292-T-A
gnomAD v4: 18-42470292-T-A
MyVariant Identifiers: chr18:g.40050257T>A (hg19) chr18:g.42470292T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470292T>A , CM000680.2:g.42470292T>A GRCh38
NC_000018.9:g.40050257T>A , CM000680.1:g.40050257T>A GRCh37
NC_000018.8:g.38304255T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15303T>A
NR_046454.1:n.652+15303T>A
NR_046455.1:n.489+15303T>A
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