Canonical Allele Identifier: CA2658964578
Gene: MSH6 HGNC NCBI

Linked Data

gnomAD v4: 2-47782956-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782956G>C , CM000664.2:g.47782956G>C GRCh38
NC_000002.11:g.48010095G>C , CM000664.1:g.48010095G>C GRCh37
NC_000002.10:g.47863599G>C NCBI36
NG_007111.1:g.4810G>C , LRG_219:g.4810G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7971G>C ENSP00000498629.1:n.-37-7971G>C
ENST00000606499.1:c.-37-7971G>C ENSP00000475605.1:n.-37-7971G>C
Search 100 bp 5'
Search 100 bp 3'