Canonical Allele Identifier: CA2495826316
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402979A= , CM000664.2:g.47402979A= GRCh38
NC_000002.11:g.47630118A= , CM000664.1:g.47630118A= GRCh37
NC_000002.10:g.47483622A= NCBI36
NG_007110.2:g.4856A= , LRG_218:g.4856A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-213A= ENSP00000233146.2:n.-213A=