Canonical Allele Identifier: CA1001241896
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1644328643
gnomAD v3: 1-45329217-C-T
gnomAD v4: 1-45329217-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329217C>T , CM000663.2:g.45329217C>T GRCh38
NC_000001.10:g.45794889C>T , CM000663.1:g.45794889C>T GRCh37
NC_000001.9:g.45567476C>T NCBI36
NG_008189.1:g.16254G>A , LRG_220:g.16254G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*89G>A ENSP00000437093.1:n.*89G>A
Search 100 bp 5'
Search 100 bp 3'