Canonical Allele Identifier: CA2496037698
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782928G= , CM000664.2:g.47782928G= GRCh38
NC_000002.11:g.48010067G= , CM000664.1:g.48010067G= GRCh37
NC_000002.10:g.47863571G= NCBI36
NG_007111.1:g.4782G= , LRG_219:g.4782G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7999G= ENSP00000498629.1:n.-37-7999G=
ENST00000606499.1:c.-37-7999G= ENSP00000475605.1:n.-37-7999G=