Canonical Allele Identifier: CA2495826393
Gene: MSH2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403067A= , CM000664.2:g.47403067A= GRCh38
NC_000002.11:g.47630206A= , CM000664.1:g.47630206A= GRCh37
NC_000002.10:g.47483710A= NCBI36
NG_007110.2:g.4944A= , LRG_218:g.4944A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-139A= ENSP00000442697.1:n.-139A=
ENST00000233146.6:c.-125A= ENSP00000233146.2:n.-125A=
ENST00000454849.5:c.-139A= ENSP00000411482.1:n.-139A=
ENST00000543555.5:c.-139A= ENSP00000442697.1:n.-139A=
NM_000251.2:c.-125A= , LRG_218t1:c.-125A= NP_000242.1:n.-125A=
NM_001258281.1:c.-139A= NP_001245210.1:n.-139A=
Search 100 bp 5'
Search 100 bp 3'