Canonical Allele Identifier: CA2495826417
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403094C= , CM000664.2:g.47403094C= GRCh38
NC_000002.11:g.47630233C= , CM000664.1:g.47630233C= GRCh37
NC_000002.10:g.47483737C= NCBI36
NG_007110.2:g.4971C= , LRG_218:g.4971C=

Transcript Alleles

HGVS Amino-acid change
ENST00000543555.6:c.-112C= ENSP00000442697.1:n.-112C=
ENST00000233146.6:c.-98C= ENSP00000233146.2:n.-98C=
ENST00000454849.5:c.-112C= ENSP00000411482.1:n.-112C=
ENST00000543555.5:c.-112C= ENSP00000442697.1:n.-112C=
NM_000251.2:c.-98C= , LRG_218t1:c.-98C= NP_000242.1:n.-98C=
NM_001258281.1:c.-112C= NP_001245210.1:n.-112C=