Canonical Allele Identifier: CA2495826328
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402991T= , CM000664.2:g.47402991T= GRCh38
NC_000002.11:g.47630130T= , CM000664.1:g.47630130T= GRCh37
NC_000002.10:g.47483634T= NCBI36
NG_007110.2:g.4868T= , LRG_218:g.4868T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-201T= ENSP00000233146.2:n.-201T=