Canonical Allele Identifier: CA2699103537
Gene: MSH2 HGNC NCBI

Linked Data

dbSNP Id: rs1238007479
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403033C>G , CM000664.2:g.47403033C>G GRCh38
NC_000002.11:g.47630172C>G , CM000664.1:g.47630172C>G GRCh37
NC_000002.10:g.47483676C>G NCBI36
NG_007110.2:g.4910C>G , LRG_218:g.4910C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-159C>G ENSP00000233146.2:n.-159C>G
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