Canonical Allele Identifier: CA2699138479

Gene: MSH2

Linked Data

• dbSNP Id: rs1672212189

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403035G>C , CM000664.2:g.47403035G>C	GRCh38
NC_000002.11:g.47630174G>C , CM000664.1:g.47630174G>C	GRCh37
NC_000002.10:g.47483678G>C	NCBI36
NG_007110.2:g.4912G>C , LRG_218:g.4912G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-157G>C	ENSP00000233146.2:n.-157G>C