Canonical Allele Identifier: CA2496037825
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668092957

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783048dup , CM000664.2:g.47783048dup GRCh38
NC_000002.11:g.48010187dup , CM000664.1:g.48010187dup GRCh37
NC_000002.10:g.47863691dup NCBI36
NG_007111.1:g.4902dup , LRG_219:g.4902dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7879dup ENSP00000498629.1:n.-37-7879dup
ENST00000606499.1:c.-37-7879dup ENSP00000475605.1:n.-37-7879dup