Canonical Allele Identifier: CA020085
Gene: MSH2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 90893
ClinVar RCV Id: RCV000076395
dbSNP Id: rs267607917

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47408399A>G , CM000664.2:g.47408399A>G GRCh38
NC_000002.11:g.47635538A>G , CM000664.1:g.47635538A>G GRCh37
NC_000002.10:g.47489042A>G NCBI36
NG_007110.2:g.10276A>G , LRG_218:g.10276A>G

Transcript Alleles

HGVS Amino-acid change
NM_000251.2:c.212-2A>G , LRG_218t1:c.212-2A>G NP_000242.1:p.=
NM_001258281.1:c.14-2A>G VV NP_001245210.1:p.=
XM_005264332.2:c.212-2A>G XP_005264389.2:p.=
XM_011532867.1:c.212-2A>G XP_011531169.1:p.=
XR_939685.1:n.284-2A>G
XM_005264332.4:c.212-2A>G XP_005264389.2:p.=
XM_011532867.2:c.212-2A>G XP_011531169.1:p.=
XR_001738747.2:n.274-2A>G
XR_939685.2:n.274-2A>G
ENST00000233146.6:c.212-2A>G ENSP00000233146.2:p.=
ENST00000406134.5:c.212-2A>G ENSP00000384199.1:p.=
ENST00000454849.5:c.14-2A>G ENSP00000411482.1:p.=
ENST00000543555.5:c.14-2A>G ENSP00000442697.1:p.=
ENST00000610696.4:c.212-2A>G ENSP00000483159.1:p.=
ENST00000613514.4:c.212-2A>G ENSP00000484137.1:p.=
ENST00000617333.3:c.212-2A>G ENSP00000482468.1:p.=
ENST00000617938.4:c.212-2A>G ENSP00000481158.1:p.=
ENST00000621359.2:c.212-2A>G ENSP00000481416.1:p.=