Canonical Allele Identifier: CA736160847
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1190188668
gnomAD v3: 1-45329209-G-A
gnomAD v4: 1-45329209-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329209G>A , CM000663.2:g.45329209G>A GRCh38
NC_000001.10:g.45794881G>A , CM000663.1:g.45794881G>A GRCh37
NC_000001.9:g.45567468G>A NCBI36
NG_008189.1:g.16262C>T , LRG_220:g.16262C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*97C>T ENSP00000437093.1:n.*97C>T