Canonical Allele Identifier: CA1030294134
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668078684

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782893del , CM000664.2:g.47782893del GRCh38
NC_000002.11:g.48010032del , CM000664.1:g.48010032del GRCh37
NC_000002.10:g.47863536del NCBI36
NG_007111.1:g.4747del , LRG_219:g.4747del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-8034del ENSP00000498629.1:n.-37-8034del
ENST00000606499.1:c.-37-8034del ENSP00000475605.1:n.-37-8034del