Canonical Allele Identifier: CA299441745
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs113232616
gnomAD v2: 18-40050351-G-A
gnomAD v3: 18-42470386-G-A
gnomAD v4: 18-42470386-G-A
MyVariant Identifiers: chr18:g.40050351G>A (hg19) chr18:g.42470386G>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+15397G>A
NR_046454.1:n.652+15397G>A
NR_046455.1:n.489+15397G>A
Search 100 bp 5'
Search 100 bp 3'