Canonical Allele Identifier: CA1357864571
Gene: MLH1 HGNC NCBI
EPM2AIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798893
ClinVar RCV Id: RCV002435864
dbSNP Id: rs2080858485

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993247C>T , CM000665.2:g.36993247C>T GRCh38
NC_000003.11:g.37034738C>T , CM000665.1:g.37034738C>T GRCh37
NC_000003.10:g.37009742C>T NCBI36
NG_007109.2:g.4898C>T , LRG_216:g.4898C>T
NG_008418.1:g.5058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673673.2:c.-301C>T (MLH1) ENSP00000500979.2:n.-301C>T
NM_014805.3:c.-170G>A (EPM2AIP1) NP_055620.1:n.-170G>A