Canonical Allele Identifier: CA2699221333

Gene: MSH2

Linked Data

• dbSNP Id: rs2103860665

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403081T>G , CM000664.2:g.47403081T>G	GRCh38
NC_000002.11:g.47630220T>G , CM000664.1:g.47630220T>G	GRCh37
NC_000002.10:g.47483724T>G	NCBI36
NG_007110.2:g.4958T>G , LRG_218:g.4958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543555.6:c.-125T>G	ENSP00000442697.1:n.-125T>G
ENST00000233146.6:c.-111T>G	ENSP00000233146.2:n.-111T>G
ENST00000454849.5:c.-125T>G	ENSP00000411482.1:n.-125T>G
ENST00000543555.5:c.-125T>G	ENSP00000442697.1:n.-125T>G
NM_000251.2:c.-111T>G , LRG_218t1:c.-111T>G	NP_000242.1:n.-111T>G
NM_001258281.1:c.-125T>G	NP_001245210.1:n.-125T>G