Canonical Allele Identifier: CA2658965019
Gene: MSH6 HGNC NCBI

Linked Data

gnomAD v4: 2-47783118-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783118T>A , CM000664.2:g.47783118T>A GRCh38
NC_000002.11:g.48010257T>A , CM000664.1:g.48010257T>A GRCh37
NC_000002.10:g.47863761T>A NCBI36
NG_007111.1:g.4972T>A , LRG_219:g.4972T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7809T>A ENSP00000498629.1:n.-37-7809T>A
ENST00000234420.9:c.-116T>A ENSP00000234420.4:n.-116T>A
ENST00000445503.5:c.-116T>A ENSP00000405294.1:n.-116T>A
ENST00000540021.5:c.-116T>A ENSP00000446475.1:n.-116T>A
ENST00000606499.1:c.-37-7809T>A ENSP00000475605.1:n.-37-7809T>A
ENST00000614496.4:c.-852T>A ENSP00000477844.1:n.-852T>A
ENST00000622629.4:c.-3212T>A ENSP00000482078.1:n.-3212T>A
NM_000179.2:c.-116T>A , LRG_219t1:c.-116T>A NP_000170.1:n.-116T>A
NM_001281492.1:c.-116T>A NP_001268421.1:n.-116T>A
NM_001281493.1:c.-852T>A NP_001268422.1:n.-852T>A
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