Canonical Allele Identifier: CA2495826379
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403055A= , CM000664.2:g.47403055A= GRCh38
NC_000002.11:g.47630194A= , CM000664.1:g.47630194A= GRCh37
NC_000002.10:g.47483698A= NCBI36
NG_007110.2:g.4932A= , LRG_218:g.4932A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-137A= ENSP00000233146.2:n.-137A=