Canonical Allele Identifier: CA16610820

Gene: MSH2

Linked Data

• ClinVar Variation Id: 408517
• ClinVar RCV Id: RCV002230364
• dbSNP Id: rs1060502018
• MyVariant Identifiers: chr2:g.47702415A>C (hg19) ; chr2:g.47475276A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475276A>C , CM000664.2:g.47475276A>C	GRCh38
NC_000002.11:g.47702415A>C , CM000664.1:g.47702415A>C	GRCh37
NC_000002.10:g.47555919A>C	NCBI36
NG_007110.2:g.77153A>C , LRG_218:g.77153A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2005+6A>C	ENSP00000495641.2:n.2005+6A>C
ENST00000233146.7:c.2005+6A>C MANE Select	ENSP00000233146.2:n.2005+6A>C
ENST00000543555.6:c.1807+6A>C	ENSP00000442697.1:n.1807+6A>C
ENST00000644092.1:c.*305+6A>C	ENSP00000496351.1:n.*305+6A>C
ENST00000645339.1:c.2005+6A>C	ENSP00000496441.1:n.2005+6A>C
ENST00000645506.1:c.2005+6A>C	ENSP00000495455.1:n.2005+6A>C
ENST00000646415.1:c.2005+6A>C	ENSP00000495543.1:n.2005+6A>C
ENST00000233146.6:c.2005+6A>C	ENSP00000233146.2:n.2005+6A>C
ENST00000406134.5:c.2005+6A>C	ENSP00000384199.1:n.2005+6A>C
ENST00000543555.5:c.1807+6A>C	ENSP00000442697.1:n.1807+6A>C
ENST00000610696.4:c.*401+6A>C	ENSP00000483159.1:n.*401+6A>C
ENST00000613514.4:c.*545+6A>C	ENSP00000484137.1:n.*545+6A>C
ENST00000617333.3:c.*771+6A>C	ENSP00000482468.1:n.*771+6A>C
ENST00000617938.4:c.*977+6A>C	ENSP00000481158.1:n.*977+6A>C
ENST00000621359.2:c.2005+6A>C	ENSP00000481416.1:n.2005+6A>C
NM_000251.2:c.2005+6A>C , LRG_218t1:c.2005+6A>C	NP_000242.1:n.2005+6A>C
NM_001258281.1:c.1807+6A>C	NP_001245210.1:n.1807+6A>C
XM_005264332.2:c.2005+6A>C	XP_005264389.2:n.2005+6A>C
XM_011532867.1:c.2005+6A>C	XP_011531169.1:n.2005+6A>C
XR_939685.1:n.2077+6A>C
XM_005264332.4:c.2005+6A>C	XP_005264389.2:n.2005+6A>C
XM_011532867.2:c.2005+6A>C	XP_011531169.1:n.2005+6A>C
XR_001738747.2:n.2067+6A>C
XR_939685.2:n.2067+6A>C
NM_000251.3:c.2005+6A>C MANE Select	NP_000242.1:n.2005+6A>C