Canonical Allele Identifier: CA2237553628
Gene: MPHOSPH6 HGNC NCBI

Linked Data

dbSNP Id: rs1906152500
gnomAD v4: 16-82148488-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148488C>T , CM000678.2:g.82148488C>T GRCh38
NC_000016.9:g.82182093C>T , CM000678.1:g.82182093C>T GRCh37
NC_000016.8:g.80739594C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*243G>A MANE Select ENSP00000258169.4:n.*243G>A
ENST00000258169.8:c.*243G>A ENSP00000258169.4:n.*243G>A
ENST00000563100.5:c.*72+171G>A ENSP00000454996.1:n.*72+171G>A
NM_005792.2:c.*243G>A MANE Select NP_005783.2:n.*243G>A
XM_011522808.1:c.*243G>A XP_011521110.1:n.*243G>A
XM_011522808.3:c.*243G>A XP_011521110.1:n.*243G>A
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