Canonical Allele Identifier: CA1887353468
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1834811659
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677557C>T , CM000672.2:g.4677557C>T GRCh38
NC_000010.10:g.4719749C>T , CM000672.1:g.4719749C>T GRCh37
NC_000010.9:g.4709749C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+492G>A
XR_930595.1:n.1911+738C>T
XR_930596.1:n.1900+738C>T
XR_001747338.1:n.1911+738C>T
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