Canonical Allele Identifier: CA2658965023

Gene: MSH6

Linked Data

• gnomAD v4: 2-47783119-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783119T>G , CM000664.2:g.47783119T>G	GRCh38
NC_000002.11:g.48010258T>G , CM000664.1:g.48010258T>G	GRCh37
NC_000002.10:g.47863762T>G	NCBI36
NG_007111.1:g.4973T>G , LRG_219:g.4973T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7808T>G	ENSP00000498629.1:n.-37-7808T>G
ENST00000234420.9:c.-115T>G	ENSP00000234420.4:n.-115T>G
ENST00000445503.5:c.-115T>G	ENSP00000405294.1:n.-115T>G
ENST00000540021.5:c.-115T>G	ENSP00000446475.1:n.-115T>G
ENST00000606499.1:c.-37-7808T>G	ENSP00000475605.1:n.-37-7808T>G
ENST00000614496.4:c.-851T>G	ENSP00000477844.1:n.-851T>G
ENST00000622629.4:c.-3211T>G	ENSP00000482078.1:n.-3211T>G
NM_000179.2:c.-115T>G , LRG_219t1:c.-115T>G	NP_000170.1:n.-115T>G
NM_001281492.1:c.-115T>G	NP_001268421.1:n.-115T>G
NM_001281493.1:c.-851T>G	NP_001268422.1:n.-851T>G