Canonical Allele Identifier: CA2496037702
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782932T= , CM000664.2:g.47782932T= GRCh38
NC_000002.11:g.48010071T= , CM000664.1:g.48010071T= GRCh37
NC_000002.10:g.47863575T= NCBI36
NG_007111.1:g.4786T= , LRG_219:g.4786T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7995T= ENSP00000498629.1:n.-37-7995T=
ENST00000606499.1:c.-37-7995T= ENSP00000475605.1:n.-37-7995T=