Canonical Allele Identifier: CA2658964641
Gene: MSH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782994_47782995del , CM000664.2:g.47782994_47782995del GRCh38
NC_000002.11:g.48010133_48010134del , CM000664.1:g.48010133_48010134del GRCh37
NC_000002.10:g.47863637_47863638del NCBI36
NG_007111.1:g.4848_4849del , LRG_219:g.4848_4849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7933_-37-7932del ENSP00000498629.1:n.-37-7933_-37-7932del
ENST00000606499.1:c.-37-7933_-37-7932del ENSP00000475605.1:n.-37-7933_-37-7932del