Canonical Allele Identifier: CA665688151
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1308969176
gnomAD v3: 10-4677543-A-T
gnomAD v4: 10-4677543-A-T
MyVariant Identifiers: chr10:g.4719735A>T (hg19) chr10:g.4677543A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677543A>T , CM000672.2:g.4677543A>T GRCh38
NC_000010.10:g.4719735A>T , CM000672.1:g.4719735A>T GRCh37
NC_000010.9:g.4709735A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+506T>A
XR_930595.1:n.1911+724A>T
XR_930596.1:n.1900+724A>T
XR_001747338.1:n.1911+724A>T
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