Canonical Allele Identifier: CA299441757
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs189858992
gnomAD v2: 18-40050492-C-T
gnomAD v3: 18-42470527-C-T
gnomAD v4: 18-42470527-C-T
MyVariant Identifiers: chr18:g.40050492C>T (hg19) chr18:g.42470527C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470527C>T , CM000680.2:g.42470527C>T GRCh38
NC_000018.9:g.40050492C>T , CM000680.1:g.40050492C>T GRCh37
NC_000018.8:g.38304490C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15538C>T
NR_046454.1:n.652+15538C>T
NR_046455.1:n.489+15538C>T
Search 100 bp 5'
Search 100 bp 3'