Canonical Allele Identifier: CA2496037705
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668082191

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782936_47782937del , CM000664.2:g.47782936_47782937del GRCh38
NC_000002.11:g.48010075_48010076del , CM000664.1:g.48010075_48010076del GRCh37
NC_000002.10:g.47863579_47863580del NCBI36
NG_007111.1:g.4790_4791del , LRG_219:g.4790_4791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7991_-37-7990del ENSP00000498629.1:n.-37-7991_-37-7990del
ENST00000606499.1:c.-37-7991_-37-7990del ENSP00000475605.1:n.-37-7991_-37-7990del