Canonical Allele Identifier: CA2658943742
Gene: MSH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403037_47403038insACCAATCATAAGCAGACGCGGCA , CM000664.2:g.47403037_47403038insACCAATCATAAGCAGACGCGGCA GRCh38
NC_000002.11:g.47630176_47630177insACCAATCATAAGCAGACGCGGCA , CM000664.1:g.47630176_47630177insACCAATCATAAGCAGACGCGGCA GRCh37
NC_000002.10:g.47483680_47483681insACCAATCATAAGCAGACGCGGCA NCBI36
NG_007110.2:g.4914_4915insACCAATCATAAGCAGACGCGGCA , LRG_218:g.4914_4915insACCAATCATAAGCAGACGCGGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-155_-154insACCAATCATAAGCAGACGCGGCA ENSP00000233146.2:n.-155_-154insACCAATCATAAGCAGACGCGGCA