Canonical Allele Identifier: CA46686865
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs910949968
MyVariant Identifiers: chr2:g.47782938G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782938G>A , CM000664.2:g.47782938G>A GRCh38
NC_000002.11:g.48010077G>A , CM000664.1:g.48010077G>A GRCh37
NC_000002.10:g.47863581G>A NCBI36
NG_007111.1:g.4792G>A , LRG_219:g.4792G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7989G>A ENSP00000498629.1:n.-37-7989G>A
ENST00000606499.1:c.-37-7989G>A ENSP00000475605.1:n.-37-7989G>A
Search 100 bp 5'
Search 100 bp 3'