Canonical Allele Identifier: CA665688192
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1387993931
gnomAD v3: 10-4677584-A-G
gnomAD v4: 10-4677584-A-G
MyVariant Identifiers: chr10:g.4719776A>G (hg19) chr10:g.4677584A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677584A>G , CM000672.2:g.4677584A>G GRCh38
NC_000010.10:g.4719776A>G , CM000672.1:g.4719776A>G GRCh37
NC_000010.9:g.4709776A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024475.1:n.22+465T>C
XR_930595.1:n.1911+765A>G
XR_930596.1:n.1900+765A>G
XR_001747338.1:n.1911+765A>G
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