Canonical Allele Identifier: CA769468033
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1317339243
MyVariant Identifiers: chr2:g.48010023G>A (hg19) chr2:g.47782884G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782884G>A , CM000664.2:g.47782884G>A GRCh38
NC_000002.11:g.48010023G>A , CM000664.1:g.48010023G>A GRCh37
NC_000002.10:g.47863527G>A NCBI36
NG_007111.1:g.4738G>A , LRG_219:g.4738G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-8043G>A ENSP00000498629.1:n.-37-8043G>A
ENST00000606499.1:c.-37-8043G>A ENSP00000475605.1:n.-37-8043G>A
Search 100 bp 5'
Search 100 bp 3'