Canonical Allele Identifier: CA736160855
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1249010902
gnomAD v3: 1-45329213-C-T
gnomAD v4: 1-45329213-C-T
MyVariant Identifiers: chr1:g.45794885C>T (hg19) chr1:g.45329213C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329213C>T , CM000663.2:g.45329213C>T GRCh38
NC_000001.10:g.45794885C>T , CM000663.1:g.45794885C>T GRCh37
NC_000001.9:g.45567472C>T NCBI36
NG_008189.1:g.16258G>A , LRG_220:g.16258G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529984.5:c.*93G>A ENSP00000437093.1:n.*93G>A
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