Canonical Allele Identifier: CA2658964980

Gene: MSH6

Linked Data

• gnomAD v4: 2-47783101-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783101G>T , CM000664.2:g.47783101G>T	GRCh38
NC_000002.11:g.48010240G>T , CM000664.1:g.48010240G>T	GRCh37
NC_000002.10:g.47863744G>T	NCBI36
NG_007111.1:g.4955G>T , LRG_219:g.4955G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7826G>T	ENSP00000498629.1:n.-37-7826G>T
ENST00000234420.9:c.-133G>T	ENSP00000234420.4:n.-133G>T
ENST00000445503.5:c.-133G>T	ENSP00000405294.1:n.-133G>T
ENST00000540021.5:c.-133G>T	ENSP00000446475.1:n.-133G>T
ENST00000606499.1:c.-37-7826G>T	ENSP00000475605.1:n.-37-7826G>T
ENST00000614496.4:c.-869G>T	ENSP00000477844.1:n.-869G>T
ENST00000622629.4:c.-3229G>T	ENSP00000482078.1:n.-3229G>T
NM_000179.2:c.-133G>T , LRG_219t1:c.-133G>T	NP_000170.1:n.-133G>T
NM_001281492.1:c.-133G>T	NP_001268421.1:n.-133G>T
NM_001281493.1:c.-869G>T	NP_001268422.1:n.-869G>T