Canonical Allele Identifier: CA2580069286
Gene: MLH1 HGNC NCBI
EPM2AIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798492
ClinVar RCV Id: RCV002442306

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993250A>G , CM000665.2:g.36993250A>G GRCh38
NC_000003.11:g.37034741A>G , CM000665.1:g.37034741A>G GRCh37
NC_000003.10:g.37009745A>G NCBI36
NG_007109.2:g.4901A>G , LRG_216:g.4901A>G
NG_008418.1:g.5055T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673673.2:c.-298A>G (MLH1) ENSP00000500979.2:n.-298A>G
NM_014805.3:c.-173T>C (EPM2AIP1) NP_055620.1:n.-173T>C