Canonical Allele Identifier: CA14627134
Gene: LINC00907 HGNC NCBI
dbSNP:
7231412
gnomAD v2:
18:40105657 T / C
gnomAD v3:
18:42525692 T / C
gnomAD v4:
chr18-42525692-T-C
Joint Max Group AF 0.42998795 (EAS)
Genomes Max Group AF 0.42998795 (EAS)
MyVariant.info:
GRCh38 chr18:g.42525692T>C
GRCh37 chr18:g.40105657T>C
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42525692T>C , CM000680.2:g.42525692T>C GRCh38
NC_000018.9:g.40105657T>C , CM000680.1:g.40105657T>C GRCh37
NC_000018.8:g.38359655T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.873-49101T>C
NR_046454.1:n.704-7427T>C
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