Canonical Allele Identifier: CA1887353489
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1834812237
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677602C>A , CM000672.2:g.4677602C>A GRCh38
NC_000010.10:g.4719794C>A , CM000672.1:g.4719794C>A GRCh37
NC_000010.9:g.4709794C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024475.1:n.22+447G>T
XR_930595.1:n.1911+783C>A
XR_930596.1:n.1900+783C>A
XR_001747338.1:n.1911+783C>A
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