Canonical Allele Identifier: CA769443105

Gene: MSH2

Linked Data

• dbSNP Id: rs1173342374
• MyVariant Identifiers: chr2:g.47630129G>T (hg19) ; chr2:g.47402990G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47402990G>T , CM000664.2:g.47402990G>T	GRCh38
NC_000002.11:g.47630129G>T , CM000664.1:g.47630129G>T	GRCh37
NC_000002.10:g.47483633G>T	NCBI36
NG_007110.2:g.4867G>T , LRG_218:g.4867G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-202G>T	ENSP00000233146.2:n.-202G>T