Canonical Allele Identifier: CA021770

Gene: MSH2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403011G>A , CM000664.2:g.47403011G>A	GRCh38
NC_000002.11:g.47630150G>A , CM000664.1:g.47630150G>A	GRCh37
NC_000002.10:g.47483654G>A	NCBI36
NG_007110.2:g.4888G>A , LRG_218:g.4888G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-181G>A	ENSP00000233146.2:n.-181G>A