Canonical Allele Identifier: CA2580066612
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1787062
ClinVar RCV Id: RCV002432712

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402976del , CM000664.2:g.47402976del GRCh38
NC_000002.11:g.47630115del , CM000664.1:g.47630115del GRCh37
NC_000002.10:g.47483619del NCBI36
NG_007110.2:g.4853del , LRG_218:g.4853del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-216del ENSP00000233146.2:n.-216del