Canonical Allele Identifier: CA2580066612

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1787062
• ClinVar RCV Id: RCV002432712
• gnomAD v4: 2-47402975-GC-G

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