Canonical Allele Identifier: CA623789956
Gene: MPHOSPH6 HGNC NCBI

Linked Data

dbSNP Id: rs1211078633

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148455A>C , CM000678.2:g.82148455A>C GRCh38
NC_000016.9:g.82182060A>C , CM000678.1:g.82182060A>C GRCh37
NC_000016.8:g.80739561A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*276T>G MANE Select ENSP00000258169.4:n.*276T>G
ENST00000258169.8:c.*276T>G ENSP00000258169.4:n.*276T>G
ENST00000563100.5:c.*72+204T>G ENSP00000454996.1:n.*72+204T>G
NM_005792.2:c.*276T>G MANE Select NP_005783.2:n.*276T>G
XM_011522808.1:c.*276T>G XP_011521110.1:n.*276T>G
XM_011522808.3:c.*276T>G XP_011521110.1:n.*276T>G