Canonical Allele Identifier: CA2496037883

Gene: MSH6

Linked Data

• dbSNP Id: rs1668098292

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783100T>A , CM000664.2:g.47783100T>A	GRCh38
NC_000002.11:g.48010239T>A , CM000664.1:g.48010239T>A	GRCh37
NC_000002.10:g.47863743T>A	NCBI36
NG_007111.1:g.4954T>A , LRG_219:g.4954T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7827T>A	ENSP00000498629.1:n.-37-7827T>A
ENST00000234420.9:c.-134T>A	ENSP00000234420.4:n.-134T>A
ENST00000445503.5:c.-134T>A	ENSP00000405294.1:n.-134T>A
ENST00000540021.5:c.-134T>A	ENSP00000446475.1:n.-134T>A
ENST00000606499.1:c.-37-7827T>A	ENSP00000475605.1:n.-37-7827T>A
ENST00000614496.4:c.-870T>A	ENSP00000477844.1:n.-870T>A
ENST00000622629.4:c.-3230T>A	ENSP00000482078.1:n.-3230T>A
NM_000179.2:c.-134T>A , LRG_219t1:c.-134T>A	NP_000170.1:n.-134T>A
NM_001281492.1:c.-134T>A	NP_001268421.1:n.-134T>A
NM_001281493.1:c.-870T>A	NP_001268422.1:n.-870T>A