Canonical Allele Identifier: CA020884

Gene: MSH2

Linked Data

• ClinVar Variation Id: 187208
• ClinVar RCV Id: RCV000166913 ; RCV000484021 ; RCV001058479
• dbSNP Id: rs786203553
• MyVariant Identifiers: chr2:g.47709967C>G (hg19) ; chr2:g.47482828C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47482828C>G , CM000664.2:g.47482828C>G	GRCh38
NC_000002.11:g.47709967C>G , CM000664.1:g.47709967C>G	GRCh37
NC_000002.10:g.47563471C>G	NCBI36
NG_007110.2:g.84705C>G , LRG_218:g.84705C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+1957C>G	ENSP00000495641.2:n.2634+1957C>G
ENST00000233146.7:c.2684C>G MANE Select	ENSP00000233146.2:p.Pro895Arg
ENST00000543555.6:c.2486C>G	ENSP00000442697.1:p.Pro829Arg
ENST00000644092.1:c.*934+1957C>G	ENSP00000496351.1:n.*934+1957C>G
ENST00000644900.1:c.487+1957C>G
ENST00000645339.1:c.2634+1957C>G	ENSP00000496441.1:n.2634+1957C>G
ENST00000645506.1:c.2634+1957C>G	ENSP00000495455.1:n.2634+1957C>G
ENST00000646415.1:c.2634+1957C>G	ENSP00000495543.1:n.2634+1957C>G
ENST00000233146.6:c.2684C>G	ENSP00000233146.2:p.Pro895Arg
ENST00000406134.5:c.2634+1957C>G	ENSP00000384199.1:n.2634+1957C>G
ENST00000461394.5:n.75+1957C>G
ENST00000543555.5:c.2486C>G	ENSP00000442697.1:p.Pro829Arg
ENST00000610696.4:c.*1080C>G	ENSP00000483159.1:n.*1080C>G
ENST00000613514.4:c.*1224C>G	ENSP00000484137.1:n.*1224C>G
ENST00000617333.3:c.*1450C>G	ENSP00000482468.1:n.*1450C>G
ENST00000617938.4:c.*1656C>G	ENSP00000481158.1:n.*1656C>G
ENST00000621359.2:c.*250C>G	ENSP00000481416.1:n.*250C>G
NM_000251.2:c.2684C>G , LRG_218t1:c.2684C>G	NP_000242.1:p.Pro895Arg
NM_001258281.1:c.2486C>G	NP_001245210.1:p.Pro829Arg
XM_005264332.2:c.2634+1957C>G	XP_005264389.2:n.2634+1957C>G
XM_011532867.1:c.2634+1957C>G	XP_011531169.1:n.2634+1957C>G
XR_939685.1:n.2706+1957C>G
XM_005264332.4:c.2634+1957C>G	XP_005264389.2:n.2634+1957C>G
XM_011532867.2:c.2634+1957C>G	XP_011531169.1:n.2634+1957C>G
XR_001738747.2:n.2696+1957C>G
XR_939685.2:n.2696+1957C>G
NM_000251.3:c.2684C>G MANE Select	NP_000242.1:p.Pro895Arg