Canonical Allele Identifier: CA2749811817
Gene: MSH6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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