Canonical Allele Identifier: CA21833250
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs948369739
gnomAD v2: 1-45794888-C-G
gnomAD v3: 1-45329216-C-G
gnomAD v4: 1-45329216-C-G
MyVariant Identifiers: chr1:g.45794888C>G (hg19) chr1:g.45329216C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329216C>G , CM000663.2:g.45329216C>G GRCh38
NC_000001.10:g.45794888C>G , CM000663.1:g.45794888C>G GRCh37
NC_000001.9:g.45567475C>G NCBI36
NG_008189.1:g.16255G>C , LRG_220:g.16255G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*90G>C ENSP00000437093.1:n.*90G>C
Search 100 bp 5'
Search 100 bp 3'