Canonical Allele Identifier: CA1887353477
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1834811930

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677579G>C , CM000672.2:g.4677579G>C GRCh38
NC_000010.10:g.4719771G>C , CM000672.1:g.4719771G>C GRCh37
NC_000010.9:g.4709771G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+470C>G
XR_930595.1:n.1911+760G>C
XR_930596.1:n.1900+760G>C
XR_001747338.1:n.1911+760G>C