Canonical Allele Identifier: CA299441746
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs113232616
gnomAD v3: 18-42470386-G-T
gnomAD v4: 18-42470386-G-T
MyVariant Identifiers: chr18:g.40050351G>T (hg19) chr18:g.42470386G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470386G>T , CM000680.2:g.42470386G>T GRCh38
NC_000018.9:g.40050351G>T , CM000680.1:g.40050351G>T GRCh37
NC_000018.8:g.38304349G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15397G>T
NR_046454.1:n.652+15397G>T
NR_046455.1:n.489+15397G>T
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