Canonical Allele Identifier: CA019963

Gene: MSH2

Linked Data

• ClinVar Variation Id: 90878
• ClinVar RCV Id: RCV000076380 ; RCV000491588 ; RCV000821619
• dbSNP Id: rs63750232
• MyVariant Identifiers: chr2:g.47703574G>C (hg19) ; chr2:g.47476435G>C (hg38)
• PubMed: PMID:10612836 ; PMID:17720936 ; PMID:18383312 ; PMID:22290698 ; PMID:26951660 ; PMID:28577310

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476435G>C , CM000664.2:g.47476435G>C	GRCh38
NC_000002.11:g.47703574G>C , CM000664.1:g.47703574G>C	GRCh37
NC_000002.10:g.47557078G>C	NCBI36
NG_007110.2:g.78312G>C , LRG_218:g.78312G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2074G>C	ENSP00000495641.2:p.Gly692Arg
ENST00000233146.7:c.2074G>C MANE Select	ENSP00000233146.2:p.Gly692Arg
ENST00000543555.6:c.1876G>C	ENSP00000442697.1:p.Gly626Arg
ENST00000644092.1:c.*374G>C	ENSP00000496351.1:n.*374G>C
ENST00000645339.1:c.2074G>C	ENSP00000496441.1:p.Gly692Arg
ENST00000645506.1:c.2074G>C	ENSP00000495455.1:p.Gly692Arg
ENST00000646415.1:c.2074G>C	ENSP00000495543.1:p.Gly692Arg
ENST00000233146.6:c.2074G>C	ENSP00000233146.2:p.Gly692Arg
ENST00000406134.5:c.2074G>C	ENSP00000384199.1:p.Gly692Arg
ENST00000543555.5:c.1876G>C	ENSP00000442697.1:p.Gly626Arg
ENST00000610696.4:c.*470G>C	ENSP00000483159.1:n.*470G>C
ENST00000613514.4:c.*614G>C	ENSP00000484137.1:n.*614G>C
ENST00000617333.3:c.*840G>C	ENSP00000482468.1:n.*840G>C
ENST00000617938.4:c.*1046G>C	ENSP00000481158.1:n.*1046G>C
ENST00000621359.2:c.2074G>C	ENSP00000481416.1:p.Gly692Arg
NM_000251.2:c.2074G>C , LRG_218t1:c.2074G>C	NP_000242.1:p.Gly692Arg
NM_001258281.1:c.1876G>C	NP_001245210.1:p.Gly626Arg
XM_005264332.2:c.2074G>C	XP_005264389.2:p.Gly692Arg
XM_011532867.1:c.2074G>C	XP_011531169.1:p.Gly692Arg
XR_939685.1:n.2146G>C
XM_005264332.4:c.2074G>C	XP_005264389.2:p.Gly692Arg
XM_011532867.2:c.2074G>C	XP_011531169.1:p.Gly692Arg
XR_001738747.2:n.2136G>C
XR_939685.2:n.2136G>C
NM_000251.3:c.2074G>C MANE Select	NP_000242.1:p.Gly692Arg