Canonical Allele Identifier: CA736160857

Gene: MUTYH

Linked Data

• dbSNP Id: rs1207667368
• gnomAD v3: 1-45329238-A-T
• gnomAD v4: 1-45329238-A-T
• MyVariant Identifiers: chr1:g.45794910A>T (hg19) ; chr1:g.45329238A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45329238A>T , CM000663.2:g.45329238A>T	GRCh38
NC_000001.10:g.45794910A>T , CM000663.1:g.45794910A>T	GRCh37
NC_000001.9:g.45567497A>T	NCBI36
NG_008189.1:g.16233T>A , LRG_220:g.16233T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529984.5:c.*68T>A	ENSP00000437093.1:n.*68T>A