Canonical Allele Identifier: CA21833242
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs916887750
MyVariant Identifiers: chr1:g.45794883G>A (hg19) chr1:g.45329211G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329211G>A , CM000663.2:g.45329211G>A GRCh38
NC_000001.10:g.45794883G>A , CM000663.1:g.45794883G>A GRCh37
NC_000001.9:g.45567470G>A NCBI36
NG_008189.1:g.16260C>T , LRG_220:g.16260C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529984.5:c.*95C>T ENSP00000437093.1:n.*95C>T
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