Canonical Allele Identifier: CA2495826380

Gene: MSH2

Linked Data

• dbSNP Id: rs1672214264

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403055A>C , CM000664.2:g.47403055A>C	GRCh38
NC_000002.11:g.47630194A>C , CM000664.1:g.47630194A>C	GRCh37
NC_000002.10:g.47483698A>C	NCBI36
NG_007110.2:g.4932A>C , LRG_218:g.4932A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-137A>C	ENSP00000233146.2:n.-137A>C