Canonical Allele Identifier: CA2699220801

Gene: MSH2

Linked Data

• dbSNP Id: rs2103858565

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403043C>A , CM000664.2:g.47403043C>A	GRCh38
NC_000002.11:g.47630182C>A , CM000664.1:g.47630182C>A	GRCh37
NC_000002.10:g.47483686C>A	NCBI36
NG_007110.2:g.4920C>A , LRG_218:g.4920C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-149C>A	ENSP00000233146.2:n.-149C>A