Canonical Allele Identifier: CA2510939710

Gene: MSH2

Linked Data

• gnomAD v4: 2-47403014-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403014T>C , CM000664.2:g.47403014T>C	GRCh38
NC_000002.11:g.47630153T>C , CM000664.1:g.47630153T>C	GRCh37
NC_000002.10:g.47483657T>C	NCBI36
NG_007110.2:g.4891T>C , LRG_218:g.4891T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-178T>C	ENSP00000233146.2:n.-178T>C