Canonical Allele Identifier: CA15148683
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47617366A>G , CM000664.2:g.47617366A>G GRCh38
NC_000002.11:g.47844505A>G , CM000664.1:g.47844505A>G GRCh37
NC_000002.10:g.47698009A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644092.1:c.*1242+9785A>G ENSP00000496351.1:n.*1242+9785A>G
ENST00000645339.1:c.2753-15436A>G ENSP00000496441.1:n.2753-15436A>G
ENST00000646415.1:c.*125+9785A>G ENSP00000495543.1:n.*125+9785A>G
XR_001738747.2:n.3004+9785A>G