Canonical Allele Identifier: CA2699138486

Gene: MSH2

Linked Data

• dbSNP Id: rs1672219653

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403123A>T , CM000664.2:g.47403123A>T	GRCh38
NC_000002.11:g.47630262A>T , CM000664.1:g.47630262A>T	GRCh37
NC_000002.10:g.47483766A>T	NCBI36
NG_007110.2:g.5000A>T , LRG_218:g.5000A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543555.6:c.-83A>T	ENSP00000442697.1:n.-83A>T
ENST00000644092.1:c.-69A>T	ENSP00000496351.1:n.-69A>T
ENST00000645339.1:c.-69A>T	ENSP00000496441.1:n.-69A>T
ENST00000645506.1:c.-69A>T	ENSP00000495455.1:n.-69A>T
ENST00000646415.1:c.-69A>T	ENSP00000495543.1:n.-69A>T
ENST00000233146.6:c.-69A>T	ENSP00000233146.2:n.-69A>T
ENST00000454849.5:c.-83A>T	ENSP00000411482.1:n.-83A>T
ENST00000543555.5:c.-83A>T	ENSP00000442697.1:n.-83A>T
NM_000251.2:c.-69A>T , LRG_218t1:c.-69A>T	NP_000242.1:n.-69A>T
NM_001258281.1:c.-83A>T	NP_001245210.1:n.-83A>T
XM_005264332.2:c.-69A>T	XP_005264389.2:n.-69A>T
XM_011532867.1:c.-69A>T	XP_011531169.1:n.-69A>T
XR_939685.1:n.4A>T