Canonical Allele Identifier: CA2658964589
Gene: MSH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782964_47782981dup , CM000664.2:g.47782964_47782981dup GRCh38
NC_000002.11:g.48010103_48010120dup , CM000664.1:g.48010103_48010120dup GRCh37
NC_000002.10:g.47863607_47863624dup NCBI36
NG_007111.1:g.4818_4835dup , LRG_219:g.4818_4835dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7963_-37-7946dup ENSP00000498629.1:n.-37-7963_-37-7946dup
ENST00000606499.1:c.-37-7963_-37-7946dup ENSP00000475605.1:n.-37-7963_-37-7946dup