Canonical Allele Identifier: CA2495826425
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403100C= , CM000664.2:g.47403100C= GRCh38
NC_000002.11:g.47630239C= , CM000664.1:g.47630239C= GRCh37
NC_000002.10:g.47483743C= NCBI36
NG_007110.2:g.4977C= , LRG_218:g.4977C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-106C= ENSP00000442697.1:n.-106C=
ENST00000233146.6:c.-92C= ENSP00000233146.2:n.-92C=
ENST00000454849.5:c.-106C= ENSP00000411482.1:n.-106C=
ENST00000543555.5:c.-106C= ENSP00000442697.1:n.-106C=
NM_000251.2:c.-92C= , LRG_218t1:c.-92C= NP_000242.1:n.-92C=
NM_001258281.1:c.-106C= NP_001245210.1:n.-106C=