Canonical Allele Identifier: CA989645772
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs1907314395
gnomAD v3: 18-42470331-T-C
gnomAD v4: 18-42470331-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42470331T>C , CM000680.2:g.42470331T>C GRCh38
NC_000018.9:g.40050296T>C , CM000680.1:g.40050296T>C GRCh37
NC_000018.8:g.38304294T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046174.2:n.872+15342T>C
NR_046454.1:n.652+15342T>C
NR_046455.1:n.489+15342T>C
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