Canonical Allele Identifier: CA21833232
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1007938400
gnomAD v3: 1-45329186-G-A
gnomAD v4: 1-45329186-G-A
MyVariant Identifiers: chr1:g.45794858G>A (hg19) chr1:g.45329186G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329186G>A , CM000663.2:g.45329186G>A GRCh38
NC_000001.10:g.45794858G>A , CM000663.1:g.45794858G>A GRCh37
NC_000001.9:g.45567445G>A NCBI36
NG_008189.1:g.16285C>T , LRG_220:g.16285C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*120C>T ENSP00000437093.1:n.*120C>T
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