Canonical Allele Identifier: CA2495826351
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403020T= , CM000664.2:g.47403020T= GRCh38
NC_000002.11:g.47630159T= , CM000664.1:g.47630159T= GRCh37
NC_000002.10:g.47483663T= NCBI36
NG_007110.2:g.4897T= , LRG_218:g.4897T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-172T= ENSP00000233146.2:n.-172T=