Canonical Allele Identifier: CA924407728
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1834811599
gnomAD v3: 10-4677552-T-A
gnomAD v4: 10-4677552-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677552T>A , CM000672.2:g.4677552T>A GRCh38
NC_000010.10:g.4719744T>A , CM000672.1:g.4719744T>A GRCh37
NC_000010.9:g.4709744T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+497A>T
XR_930595.1:n.1911+733T>A
XR_930596.1:n.1900+733T>A
XR_001747338.1:n.1911+733T>A
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