Canonical Allele Identifier: CA2495826314
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402976C= , CM000664.2:g.47402976C= GRCh38
NC_000002.11:g.47630115C= , CM000664.1:g.47630115C= GRCh37
NC_000002.10:g.47483619C= NCBI36
NG_007110.2:g.4853C= , LRG_218:g.4853C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-216C= ENSP00000233146.2:n.-216C=