Canonical Allele Identifier: CA21833245
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs796654257
gnomAD v2: 1-45794884-A-AC
gnomAD v3: 1-45329212-A-AC
gnomAD v4: 1-45329212-A-AC
MyVariant Identifiers: chr1:g.45794884_45794885insC (hg19) chr1:g.45329212_45329213insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329217dup , CM000663.2:g.45329217dup GRCh38
NC_000001.10:g.45794889dup , CM000663.1:g.45794889dup GRCh37
NC_000001.9:g.45567476dup NCBI36
NG_008189.1:g.16258dup , LRG_220:g.16258dup

Transcript Alleles

HGVS Amino-acid change
ENST00000529984.5:c.*93dup ENSP00000437093.1:n.*93dup
Search 100 bp 5'
Search 100 bp 3'