Canonical Allele Identifier: CA21833255
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1020117176
gnomAD v3: 1-45329228-A-G
gnomAD v4: 1-45329228-A-G
MyVariant Identifiers: chr1:g.45794900A>G (hg19) chr1:g.45329228A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329228A>G , CM000663.2:g.45329228A>G GRCh38
NC_000001.10:g.45794900A>G , CM000663.1:g.45794900A>G GRCh37
NC_000001.9:g.45567487A>G NCBI36
NG_008189.1:g.16243T>C , LRG_220:g.16243T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*78T>C ENSP00000437093.1:n.*78T>C
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