Canonical Allele Identifier: CA2495826389
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403066G= , CM000664.2:g.47403066G= GRCh38
NC_000002.11:g.47630205G= , CM000664.1:g.47630205G= GRCh37
NC_000002.10:g.47483709G= NCBI36
NG_007110.2:g.4943G= , LRG_218:g.4943G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-126G= ENSP00000233146.2:n.-126G=