Canonical Allele Identifier: CA2496037697
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782927A= , CM000664.2:g.47782927A= GRCh38
NC_000002.11:g.48010066A= , CM000664.1:g.48010066A= GRCh37
NC_000002.10:g.47863570A= NCBI36
NG_007111.1:g.4781A= , LRG_219:g.4781A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-8000A= ENSP00000498629.1:n.-37-8000A=
ENST00000606499.1:c.-37-8000A= ENSP00000475605.1:n.-37-8000A=