Canonical Allele Identifier: CA2658964708
Gene: MSH6 HGNC NCBI

Linked Data

gnomAD v4: 2-47783021-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783021C>G , CM000664.2:g.47783021C>G GRCh38
NC_000002.11:g.48010160C>G , CM000664.1:g.48010160C>G GRCh37
NC_000002.10:g.47863664C>G NCBI36
NG_007111.1:g.4875C>G , LRG_219:g.4875C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7906C>G ENSP00000498629.1:n.-37-7906C>G
ENST00000606499.1:c.-37-7906C>G ENSP00000475605.1:n.-37-7906C>G