Canonical Allele Identifier: CA2658964841
Gene: MSH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783054_47783055dup , CM000664.2:g.47783054_47783055dup GRCh38
NC_000002.11:g.48010193_48010194dup , CM000664.1:g.48010193_48010194dup GRCh37
NC_000002.10:g.47863697_47863698dup NCBI36
NG_007111.1:g.4908_4909dup , LRG_219:g.4908_4909dup

Transcript Alleles

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