Canonical Allele Identifier: CA35538745
Gene: PPP1R12B HGNC NCBI

Linked Data

dbSNP Id: rs12734338
MyVariant Identifiers: chr1:g.202469723T>C (hg19) chr1:g.202500595T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202500595T>C , CM000663.2:g.202500595T>C GRCh38
NC_000001.10:g.202469723T>C , CM000663.1:g.202469723T>C GRCh37
NC_000001.9:g.200736346T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000704899.1:c.2490+3773T>C ENSP00000516058.1:n.2490+3773T>C
ENST00000608999.6:c.2490+3773T>C MANE Select ENSP00000476755.1:n.2490+3773T>C
ENST00000290419.9:c.168+3773T>C ENSP00000484005.1:n.168+3773T>C
ENST00000391959.5:c.2673+3773T>C ENSP00000375821.5:n.2673+3773T>C
ENST00000466273.6:c.5-1264T>C
ENST00000491336.5:c.168+3773T>C ENSP00000480852.1:n.168+3773T>C
ENST00000498070.5:n.1131-1264T>C
ENST00000608999.5:c.2490+3773T>C ENSP00000476755.1:n.2490+3773T>C
NM_002481.3:c.2490+3773T>C NP_002472.2:n.2490+3773T>C
NM_032103.2:c.168+3773T>C NP_115286.1:n.168+3773T>C
NM_032104.2:c.168+3773T>C NP_115287.1:n.168+3773T>C
XM_011509573.1:c.2674-1264T>C XP_011507875.1:n.2674-1264T>C
XM_011509574.1:c.2674-1264T>C XP_011507876.1:n.2674-1264T>C
XM_011509575.1:c.2674-1264T>C XP_011507877.1:n.2674-1264T>C
NM_001331029.1:c.2673+3773T>C NP_001317958.1:n.2673+3773T>C
XM_017001342.1:c.2673+3773T>C XP_016856831.1:n.2673+3773T>C
XM_017001343.1:c.2673+3773T>C XP_016856832.1:n.2673+3773T>C
XM_017001345.1:c.2673+3773T>C XP_016856834.1:n.2673+3773T>C
XM_017001346.1:c.2490+3773T>C XP_016856835.1:n.2490+3773T>C
XM_017001347.1:c.2490+3773T>C XP_016856836.1:n.2490+3773T>C
XM_017001348.1:c.2490+3773T>C XP_016856837.1:n.2490+3773T>C
XM_017001350.1:c.1908+3773T>C XP_016856839.1:n.1908+3773T>C
XM_017001352.1:c.168+3773T>C XP_016856841.1:n.168+3773T>C
XM_017001353.1:c.168+3773T>C XP_016856842.1:n.168+3773T>C
XM_017001354.1:c.168+3773T>C XP_016856843.1:n.168+3773T>C
XR_001737195.1:n.2824-1264T>C
XR_001737196.2:n.2824-1264T>C
XR_001737197.1:n.2824-1267T>C
XR_001737198.1:n.2641-1264T>C
XR_001737199.1:n.2641-1264T>C
XR_001737200.1:n.2641-1267T>C
XR_001737201.2:n.2641-1267T>C
XR_002956646.1:n.2823+3773T>C
NM_002481.4:c.2490+3773T>C MANE Select NP_002472.2:n.2490+3773T>C
NM_001331029.2:c.2673+3773T>C NP_001317958.1:n.2673+3773T>C
NM_032103.3:c.168+3773T>C NP_115286.1:n.168+3773T>C
NM_032104.3:c.168+3773T>C NP_115287.1:n.168+3773T>C
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