Canonical Allele Identifier: CA2495826398
Gene: MSH2 HGNC NCBI

Linked Data

dbSNP Id: rs1672216030

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403078dup , CM000664.2:g.47403078dup GRCh38
NC_000002.11:g.47630217dup , CM000664.1:g.47630217dup GRCh37
NC_000002.10:g.47483721dup NCBI36
NG_007110.2:g.4955dup , LRG_218:g.4955dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-128dup ENSP00000442697.1:n.-128dup
ENST00000233146.6:c.-114dup ENSP00000233146.2:n.-114dup
ENST00000454849.5:c.-128dup ENSP00000411482.1:n.-128dup
ENST00000543555.5:c.-128dup ENSP00000442697.1:n.-128dup
NM_000251.2:c.-114dup , LRG_218t1:c.-114dup NP_000242.1:n.-114dup
NM_001258281.1:c.-128dup NP_001245210.1:n.-128dup