Canonical Allele Identifier: CA906755387
Gene: MLH1 HGNC NCBI

Linked Data

dbSNP Id: rs1308610365
gnomAD v4: 3-36993323-C-T
MyVariant Identifiers: chr3:g.37034814C>T (hg19) chr3:g.36993323C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36993323C>T , CM000665.2:g.36993323C>T GRCh38
NC_000003.11:g.37034814C>T , CM000665.1:g.37034814C>T GRCh37
NC_000003.10:g.37009818C>T NCBI36
NG_007109.2:g.4974C>T , LRG_216:g.4974C>T
NG_008418.1:g.4982G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673673.2:c.-225C>T ENSP00000500979.2:n.-225C>T
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