Canonical Allele Identifier: CA2658943676
Gene: MSH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403014_47403036del , CM000664.2:g.47403014_47403036del GRCh38
NC_000002.11:g.47630153_47630175del , CM000664.1:g.47630153_47630175del GRCh37
NC_000002.10:g.47483657_47483679del NCBI36
NG_007110.2:g.4891_4913del , LRG_218:g.4891_4913del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-178_-156del ENSP00000233146.2:n.-178_-156del