Canonical Allele Identifier: CA46687075
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1031301275
gnomAD v4: 2-47783048-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783048C>T , CM000664.2:g.47783048C>T GRCh38
NC_000002.11:g.48010187C>T , CM000664.1:g.48010187C>T GRCh37
NC_000002.10:g.47863691C>T NCBI36
NG_007111.1:g.4902C>T , LRG_219:g.4902C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7879C>T ENSP00000498629.1:n.-37-7879C>T
ENST00000606499.1:c.-37-7879C>T ENSP00000475605.1:n.-37-7879C>T