Canonical Allele Identifier: CA1887353452
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1834811252

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677511C>G , CM000672.2:g.4677511C>G GRCh38
NC_000010.10:g.4719703C>G , CM000672.1:g.4719703C>G GRCh37
NC_000010.9:g.4709703C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+538G>C
XR_930595.1:n.1911+692C>G
XR_930596.1:n.1900+692C>G
XR_001747338.1:n.1911+692C>G