Canonical Allele Identifier: CA2495826395

Gene: MSH2

Linked Data

• dbSNP Id: rs1672215587

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403070C>G , CM000664.2:g.47403070C>G	GRCh38
NC_000002.11:g.47630209C>G , CM000664.1:g.47630209C>G	GRCh37
NC_000002.10:g.47483713C>G	NCBI36
NG_007110.2:g.4947C>G , LRG_218:g.4947C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543555.6:c.-136C>G	ENSP00000442697.1:n.-136C>G
ENST00000233146.6:c.-122C>G	ENSP00000233146.2:n.-122C>G
ENST00000454849.5:c.-136C>G	ENSP00000411482.1:n.-136C>G
ENST00000543555.5:c.-136C>G	ENSP00000442697.1:n.-136C>G
NM_000251.2:c.-122C>G , LRG_218t1:c.-122C>G	NP_000242.1:n.-122C>G
NM_001258281.1:c.-136C>G	NP_001245210.1:n.-136C>G