Canonical Allele Identifier: CA299441756
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1056289626
gnomAD v2: 18-40050479-A-G
gnomAD v3: 18-42470514-A-G
gnomAD v4: 18-42470514-A-G
MyVariant Identifiers: chr18:g.40050479A>G (hg19) chr18:g.42470514A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470514A>G , CM000680.2:g.42470514A>G GRCh38
NC_000018.9:g.40050479A>G , CM000680.1:g.40050479A>G GRCh37
NC_000018.8:g.38304477A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15525A>G
NR_046454.1:n.652+15525A>G
NR_046455.1:n.489+15525A>G
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