Canonical Allele Identifier: CA779420762
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1183726173
MyVariant Identifiers: chr18:g.40050237G>T (hg19) chr18:g.42470272G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470272G>T , CM000680.2:g.42470272G>T GRCh38
NC_000018.9:g.40050237G>T , CM000680.1:g.40050237G>T GRCh37
NC_000018.8:g.38304235G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15283G>T
NR_046454.1:n.652+15283G>T
NR_046455.1:n.489+15283G>T
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