Canonical Allele Identifier: CA2496037829
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783049G= , CM000664.2:g.47783049G= GRCh38
NC_000002.11:g.48010188G= , CM000664.1:g.48010188G= GRCh37
NC_000002.10:g.47863692G= NCBI36
NG_007111.1:g.4903G= , LRG_219:g.4903G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7878G= ENSP00000498629.1:n.-37-7878G=
ENST00000606499.1:c.-37-7878G= ENSP00000475605.1:n.-37-7878G=