Canonical Allele Identifier: CA274826996
Gene: C15orf32 HGNC NCBI

Linked Data

dbSNP Id: rs8040009
gnomAD v2: 15-93044339-T-C
gnomAD v3: 15-92501109-T-C
gnomAD v4: 15-92501109-T-C
MyVariant Identifiers: chr15:g.93044339T>C (hg19) chr15:g.92501109T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.92501109T>C , CM000677.2:g.92501109T>C GRCh38
NC_000015.9:g.93044339T>C , CM000677.1:g.93044339T>C GRCh37
NC_000015.8:g.90845343T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001301106.1:c.*786T>C NP_001288035.1:n.*786T>C
NM_153040.2:c.*709T>C NP_694585.1:n.*709T>C
NR_161370.1:n.1718T>C
NR_161371.1:n.1756T>C
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