Canonical Allele Identifier: CA2658943524
Gene: MSH2 HGNC NCBI

Linked Data

gnomAD v4: 2-47402981-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402981G>T , CM000664.2:g.47402981G>T GRCh38
NC_000002.11:g.47630120G>T , CM000664.1:g.47630120G>T GRCh37
NC_000002.10:g.47483624G>T NCBI36
NG_007110.2:g.4858G>T , LRG_218:g.4858G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-211G>T ENSP00000233146.2:n.-211G>T
Search 100 bp 5'
Search 100 bp 3'