Canonical Allele Identifier: CA2658964843
Gene: MSH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783054_47783055del , CM000664.2:g.47783054_47783055del GRCh38
NC_000002.11:g.48010193_48010194del , CM000664.1:g.48010193_48010194del GRCh37
NC_000002.10:g.47863697_47863698del NCBI36
NG_007111.1:g.4908_4909del , LRG_219:g.4908_4909del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7873_-37-7872del ENSP00000498629.1:n.-37-7873_-37-7872del
ENST00000606499.1:c.-37-7873_-37-7872del ENSP00000475605.1:n.-37-7873_-37-7872del