Canonical Allele Identifier: CA2495826325
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402989C= , CM000664.2:g.47402989C= GRCh38
NC_000002.11:g.47630128C= , CM000664.1:g.47630128C= GRCh37
NC_000002.10:g.47483632C= NCBI36
NG_007110.2:g.4866C= , LRG_218:g.4866C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-203C= ENSP00000233146.2:n.-203C=