Canonical Allele Identifier: CA202648074

Gene: MANCR

Linked Data

• dbSNP Id: rs987321172
• gnomAD v3: 10-4677571-A-G
• gnomAD v4: 10-4677571-A-G
• MyVariant Identifiers: chr10:g.4719763A>G (hg19) ; chr10:g.4677571A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4677571A>G , CM000672.2:g.4677571A>G	GRCh38
NC_000010.10:g.4719763A>G , CM000672.1:g.4719763A>G	GRCh37
NC_000010.9:g.4709763A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_024475.1:n.22+478T>C
XR_930595.1:n.1911+752A>G
XR_930596.1:n.1900+752A>G
XR_001747338.1:n.1911+752A>G