Canonical Allele Identifier: CA2749811819
Gene: MSH6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782980C>A , CM000664.2:g.47782980C>A GRCh38
NC_000002.11:g.48010119C>A , CM000664.1:g.48010119C>A GRCh37
NC_000002.10:g.47863623C>A NCBI36
NG_007111.1:g.4834C>A , LRG_219:g.4834C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7947C>A ENSP00000498629.1:n.-37-7947C>A
ENST00000606499.1:c.-37-7947C>A ENSP00000475605.1:n.-37-7947C>A
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