Canonical Allele Identifier: CA2473711219
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1644326365
gnomAD v4: 1-45329206-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329206A>G , CM000663.2:g.45329206A>G GRCh38
NC_000001.10:g.45794878A>G , CM000663.1:g.45794878A>G GRCh37
NC_000001.9:g.45567465A>G NCBI36
NG_008189.1:g.16265T>C , LRG_220:g.16265T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*100T>C ENSP00000437093.1:n.*100T>C