Canonical Allele Identifier: CA346728533

Gene: MSH2

Linked Data

• ClinVar Variation Id: 483738
• ClinVar RCV Id: RCV001320397 ; RCV001764665
• dbSNP Id: rs879254044
• gnomAD v2: 2-47702287-G-C
• gnomAD v3: 2-47475148-G-C
• gnomAD v4: 2-47475148-G-C
• MyVariant Identifiers: chr2:g.47702287G>C (hg19) ; chr2:g.47475148G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475148G>C , CM000664.2:g.47475148G>C	GRCh38
NC_000002.11:g.47702287G>C , CM000664.1:g.47702287G>C	GRCh37
NC_000002.10:g.47555791G>C	NCBI36
NG_007110.2:g.77025G>C , LRG_218:g.77025G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.1883G>C	ENSP00000495641.2:p.Gly628Ala
ENST00000233146.7:c.1883G>C MANE Select	ENSP00000233146.2:p.Gly628Ala
ENST00000543555.6:c.1685G>C	ENSP00000442697.1:p.Gly562Ala
ENST00000644092.1:c.*183G>C	ENSP00000496351.1:n.*183G>C
ENST00000645339.1:c.1883G>C	ENSP00000496441.1:p.Gly628Ala
ENST00000645506.1:c.1883G>C	ENSP00000495455.1:p.Gly628Ala
ENST00000646415.1:c.1883G>C	ENSP00000495543.1:p.Gly628Ala
ENST00000233146.6:c.1883G>C	ENSP00000233146.2:p.Gly628Ala
ENST00000406134.5:c.1883G>C	ENSP00000384199.1:p.Gly628Ala
ENST00000543555.5:c.1685G>C	ENSP00000442697.1:p.Gly562Ala
ENST00000610696.4:c.*279G>C	ENSP00000483159.1:n.*279G>C
ENST00000613514.4:c.*423G>C	ENSP00000484137.1:n.*423G>C
ENST00000617333.3:c.*649G>C	ENSP00000482468.1:n.*649G>C
ENST00000617938.4:c.*855G>C	ENSP00000481158.1:n.*855G>C
ENST00000621359.2:c.1883G>C	ENSP00000481416.1:p.Gly628Ala
NM_000251.2:c.1883G>C , LRG_218t1:c.1883G>C	NP_000242.1:p.Gly628Ala
NM_001258281.1:c.1685G>C	NP_001245210.1:p.Gly562Ala
XM_005264332.2:c.1883G>C	XP_005264389.2:p.Gly628Ala
XM_011532867.1:c.1883G>C	XP_011531169.1:p.Gly628Ala
XR_939685.1:n.1955G>C
XM_005264332.4:c.1883G>C	XP_005264389.2:p.Gly628Ala
XM_011532867.2:c.1883G>C	XP_011531169.1:p.Gly628Ala
XR_001738747.2:n.1945G>C
XR_939685.2:n.1945G>C
NM_000251.3:c.1883G>C MANE Select	NP_000242.1:p.Gly628Ala