Canonical Allele Identifier: CA2495826372

Gene: MSH2

Linked Data

• dbSNP Id: rs786202735

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403049A>G , CM000664.2:g.47403049A>G	GRCh38
NC_000002.11:g.47630188A>G , CM000664.1:g.47630188A>G	GRCh37
NC_000002.10:g.47483692A>G	NCBI36
NG_007110.2:g.4926A>G , LRG_218:g.4926A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-143A>G	ENSP00000233146.2:n.-143A>G