Canonical Allele Identifier: CA2658943842
Gene: MSH2 HGNC NCBI

Linked Data

dbSNP Id: rs2103859541
gnomAD v4: 2-47403056-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403056C>G , CM000664.2:g.47403056C>G GRCh38
NC_000002.11:g.47630195C>G , CM000664.1:g.47630195C>G GRCh37
NC_000002.10:g.47483699C>G NCBI36
NG_007110.2:g.4933C>G , LRG_218:g.4933C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-136C>G ENSP00000233146.2:n.-136C>G
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