Canonical Allele Identifier: CA202648058
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs973276258
gnomAD v3: 10-4677526-C-T
gnomAD v4: 10-4677526-C-T
MyVariant Identifiers: chr10:g.4719718C>T (hg19) chr10:g.4677526C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677526C>T , CM000672.2:g.4677526C>T GRCh38
NC_000010.10:g.4719718C>T , CM000672.1:g.4719718C>T GRCh37
NC_000010.9:g.4709718C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+523G>A
XR_930595.1:n.1911+707C>T
XR_930596.1:n.1900+707C>T
XR_001747338.1:n.1911+707C>T
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