Canonical Allele Identifier: CA2658943753
Gene: MSH2 HGNC NCBI

Linked Data

gnomAD v4: 2-47403033-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403033C>A , CM000664.2:g.47403033C>A GRCh38
NC_000002.11:g.47630172C>A , CM000664.1:g.47630172C>A GRCh37
NC_000002.10:g.47483676C>A NCBI36
NG_007110.2:g.4910C>A , LRG_218:g.4910C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-159C>A ENSP00000233146.2:n.-159C>A