Canonical Allele Identifier: CA2658964687
Gene: MSH6 HGNC NCBI

Linked Data

gnomAD v4: 2-47783014-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783014G>A , CM000664.2:g.47783014G>A GRCh38
NC_000002.11:g.48010153G>A , CM000664.1:g.48010153G>A GRCh37
NC_000002.10:g.47863657G>A NCBI36
NG_007111.1:g.4868G>A , LRG_219:g.4868G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7913G>A ENSP00000498629.1:n.-37-7913G>A
ENST00000606499.1:c.-37-7913G>A ENSP00000475605.1:n.-37-7913G>A
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