Canonical Allele Identifier: CA665688157
Gene: MANCR HGNC NCBI

Linked Data

dbSNP Id: rs1273463332
gnomAD v3: 10-4677547-T-C
gnomAD v4: 10-4677547-T-C
MyVariant Identifiers: chr10:g.4719739T>C (hg19) chr10:g.4677547T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.4677547T>C , CM000672.2:g.4677547T>C GRCh38
NC_000010.10:g.4719739T>C , CM000672.1:g.4719739T>C GRCh37
NC_000010.9:g.4709739T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024475.1:n.22+502A>G
XR_930595.1:n.1911+728T>C
XR_930596.1:n.1900+728T>C
XR_001747338.1:n.1911+728T>C
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