Canonical Allele Identifier: CA2495826355
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403030C= , CM000664.2:g.47403030C= GRCh38
NC_000002.11:g.47630169C= , CM000664.1:g.47630169C= GRCh37
NC_000002.10:g.47483673C= NCBI36
NG_007110.2:g.4907C= , LRG_218:g.4907C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-162C= ENSP00000233146.2:n.-162C=