Canonical Allele Identifier: CA019673
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182608
dbSNP Id: rs730881784
gnomAD v2: 2-47630528-C-T
gnomAD v3: 2-47403389-C-T
gnomAD v4: 2-47403389-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403389C>T , CM000664.2:g.47403389C>T GRCh38
NC_000002.11:g.47630528C>T , CM000664.1:g.47630528C>T GRCh37
NC_000002.10:g.47484032C>T NCBI36
NG_007110.2:g.5266C>T , LRG_218:g.5266C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.198C>T ENSP00000495641.2:p.Tyr66=
ENST00000233146.7:c.198C>T MANE Select ENSP00000233146.2:p.Tyr66=
ENST00000543555.6:c.-1C>T ENSP00000442697.1:n.-1C>T
ENST00000644092.1:c.198C>T ENSP00000496351.1:p.Tyr66=
ENST00000645339.1:c.198C>T ENSP00000496441.1:p.Tyr66=
ENST00000645506.1:c.198C>T ENSP00000495455.1:p.Tyr66=
ENST00000646415.1:c.198C>T ENSP00000495543.1:p.Tyr66=
ENST00000233146.6:c.198C>T ENSP00000233146.2:p.Tyr66=
ENST00000406134.5:c.198C>T ENSP00000384199.1:p.Tyr66=
ENST00000454849.5:c.-1C>T ENSP00000411482.1:n.-1C>T
ENST00000543555.5:c.-1C>T ENSP00000442697.1:n.-1C>T
ENST00000610696.4:c.198C>T ENSP00000483159.1:p.Tyr66=
ENST00000613514.4:c.198C>T ENSP00000484137.1:p.Tyr66=
ENST00000617333.3:c.198C>T ENSP00000482468.1:p.Tyr66=
ENST00000617938.4:c.198C>T ENSP00000481158.1:p.Tyr66=
ENST00000621359.2:c.198C>T ENSP00000481416.1:p.Tyr66=
NM_000251.2:c.198C>T , LRG_218t1:c.198C>T NP_000242.1:p.Tyr66=
NM_001258281.1:c.-1C>T NP_001245210.1:n.-1C>T
XM_005264332.2:c.198C>T XP_005264389.2:p.Tyr66=
XM_011532867.1:c.198C>T XP_011531169.1:p.Tyr66=
XR_939685.1:n.270C>T
XM_005264332.4:c.198C>T XP_005264389.2:p.Tyr66=
XM_011532867.2:c.198C>T XP_011531169.1:p.Tyr66=
XR_001738747.2:n.260C>T
XR_939685.2:n.260C>T
NM_000251.3:c.198C>T MANE Select NP_000242.1:p.Tyr66=