Canonical Allele Identifier: CA2495826331
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402996G= , CM000664.2:g.47402996G= GRCh38
NC_000002.11:g.47630135G= , CM000664.1:g.47630135G= GRCh37
NC_000002.10:g.47483639G= NCBI36
NG_007110.2:g.4873G= , LRG_218:g.4873G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-196G= ENSP00000233146.2:n.-196G=