Canonical Allele Identifier: CA2496037713
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782942G= , CM000664.2:g.47782942G= GRCh38
NC_000002.11:g.48010081G= , CM000664.1:g.48010081G= GRCh37
NC_000002.10:g.47863585G= NCBI36
NG_007111.1:g.4796G= , LRG_219:g.4796G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7985G= ENSP00000498629.1:n.-37-7985G=
ENST00000606499.1:c.-37-7985G= ENSP00000475605.1:n.-37-7985G=