Canonical Allele Identifier: CA1030294304
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668095631
gnomAD v3: 2-47783073-C-T
gnomAD v4: 2-47783073-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783073C>T , CM000664.2:g.47783073C>T GRCh38
NC_000002.11:g.48010212C>T , CM000664.1:g.48010212C>T GRCh37
NC_000002.10:g.47863716C>T NCBI36
NG_007111.1:g.4927C>T , LRG_219:g.4927C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7854C>T ENSP00000498629.1:n.-37-7854C>T
ENST00000606499.1:c.-37-7854C>T ENSP00000475605.1:n.-37-7854C>T