Canonical Allele Identifier: CA2496037689
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782918G= , CM000664.2:g.47782918G= GRCh38
NC_000002.11:g.48010057G= , CM000664.1:g.48010057G= GRCh37
NC_000002.10:g.47863561G= NCBI36
NG_007111.1:g.4772G= , LRG_219:g.4772G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-8009G= ENSP00000498629.1:n.-37-8009G=
ENST00000606499.1:c.-37-8009G= ENSP00000475605.1:n.-37-8009G=