Canonical Allele Identifier: CA2495826315
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402977T= , CM000664.2:g.47402977T= GRCh38
NC_000002.11:g.47630116T= , CM000664.1:g.47630116T= GRCh37
NC_000002.10:g.47483620T= NCBI36
NG_007110.2:g.4854T= , LRG_218:g.4854T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-215T= ENSP00000233146.2:n.-215T=