Canonical Allele Identifier: CA1030294224
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668088107

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782991del , CM000664.2:g.47782991del GRCh38
NC_000002.11:g.48010130del , CM000664.1:g.48010130del GRCh37
NC_000002.10:g.47863634del NCBI36
NG_007111.1:g.4845del , LRG_219:g.4845del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7936del ENSP00000498629.1:n.-37-7936del
ENST00000606499.1:c.-37-7936del ENSP00000475605.1:n.-37-7936del