Canonical Allele Identifier: CA915942391
Gene: MLH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 821119
ClinVar RCV Id: RCV001015226
dbSNP Id: rs1350241720

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993315C>G , CM000665.2:g.36993315C>G GRCh38
NC_000003.11:g.37034806C>G , CM000665.1:g.37034806C>G GRCh37
NC_000003.10:g.37009810C>G NCBI36
NG_007109.2:g.4966C>G , LRG_216:g.4966C>G
NG_008418.1:g.4990G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673673.2:c.-233C>G ENSP00000500979.2:n.-233C>G