Canonical Allele Identifier: CA202648065

Gene: MANCR

Linked Data

• dbSNP Id: rs890231319
• MyVariant Identifiers: chr10:g.4719747A>C (hg19) ; chr10:g.4677555A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4677555A>C , CM000672.2:g.4677555A>C	GRCh38
NC_000010.10:g.4719747A>C , CM000672.1:g.4719747A>C	GRCh37
NC_000010.9:g.4709747A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_024475.1:n.22+494T>G
XR_930595.1:n.1911+736A>C
XR_930596.1:n.1900+736A>C
XR_001747338.1:n.1911+736A>C