Canonical Allele Identifier: CA2495826413
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403091G= , CM000664.2:g.47403091G= GRCh38
NC_000002.11:g.47630230G= , CM000664.1:g.47630230G= GRCh37
NC_000002.10:g.47483734G= NCBI36
NG_007110.2:g.4968G= , LRG_218:g.4968G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-115G= ENSP00000442697.1:n.-115G=
ENST00000233146.6:c.-101G= ENSP00000233146.2:n.-101G=
ENST00000454849.5:c.-115G= ENSP00000411482.1:n.-115G=
ENST00000543555.5:c.-115G= ENSP00000442697.1:n.-115G=
NM_000251.2:c.-101G= , LRG_218t1:c.-101G= NP_000242.1:n.-101G=
NM_001258281.1:c.-115G= NP_001245210.1:n.-115G=