Canonical Allele Identifier: CA2496037837
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668093831
gnomAD v4: 2-47783059-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783059C>T , CM000664.2:g.47783059C>T GRCh38
NC_000002.11:g.48010198C>T , CM000664.1:g.48010198C>T GRCh37
NC_000002.10:g.47863702C>T NCBI36
NG_007111.1:g.4913C>T , LRG_219:g.4913C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7868C>T ENSP00000498629.1:n.-37-7868C>T
ENST00000606499.1:c.-37-7868C>T ENSP00000475605.1:n.-37-7868C>T