Canonical Allele Identifier: CA426119440

Gene: MSH2

Linked Data

• ClinVar Variation Id: 923633
• ClinVar RCV Id: RCV001184460 ; RCV001421090
• dbSNP Id: rs587779090
• gnomAD v2: 2-47630471-C-G
• gnomAD v4: 2-47403332-C-G
• MyVariant Identifiers: chr2:g.47630471C>G (hg19) ; chr2:g.47403332C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403332C>G , CM000664.2:g.47403332C>G	GRCh38
NC_000002.11:g.47630471C>G , CM000664.1:g.47630471C>G	GRCh37
NC_000002.10:g.47483975C>G	NCBI36
NG_007110.2:g.5209C>G , LRG_218:g.5209C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.141C>G	ENSP00000495641.2:p.Gly47=
ENST00000233146.7:c.141C>G MANE Select	ENSP00000233146.2:p.Gly47=
ENST00000543555.6:c.-30-28C>G	ENSP00000442697.1:n.-30-28C>G
ENST00000644092.1:c.141C>G	ENSP00000496351.1:p.Gly47=
ENST00000645339.1:c.141C>G	ENSP00000496441.1:p.Gly47=
ENST00000645506.1:c.141C>G	ENSP00000495455.1:p.Gly47=
ENST00000646415.1:c.141C>G	ENSP00000495543.1:p.Gly47=
ENST00000233146.6:c.141C>G	ENSP00000233146.2:p.Gly47=
ENST00000406134.5:c.141C>G	ENSP00000384199.1:p.Gly47=
ENST00000454849.5:c.-30-28C>G	ENSP00000411482.1:n.-30-28C>G
ENST00000543555.5:c.-30-28C>G	ENSP00000442697.1:n.-30-28C>G
ENST00000610696.4:c.141C>G	ENSP00000483159.1:p.Gly47=
ENST00000613514.4:c.141C>G	ENSP00000484137.1:p.Gly47=
ENST00000617333.3:c.141C>G	ENSP00000482468.1:p.Gly47=
ENST00000617938.4:c.141C>G	ENSP00000481158.1:p.Gly47=
ENST00000621359.2:c.141C>G	ENSP00000481416.1:p.Gly47=
NM_000251.2:c.141C>G , LRG_218t1:c.141C>G	NP_000242.1:p.Gly47=
NM_001258281.1:c.-30-28C>G	NP_001245210.1:n.-30-28C>G
XM_005264332.2:c.141C>G	XP_005264389.2:p.Gly47=
XM_011532867.1:c.141C>G	XP_011531169.1:p.Gly47=
XR_939685.1:n.213C>G
XM_005264332.4:c.141C>G	XP_005264389.2:p.Gly47=
XM_011532867.2:c.141C>G	XP_011531169.1:p.Gly47=
XR_001738747.2:n.203C>G
XR_939685.2:n.203C>G
NM_000251.3:c.141C>G MANE Select	NP_000242.1:p.Gly47=