Canonical Allele Identifier: CA1919627384
Gene: PPP3CB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73475068C>G , CM000672.2:g.73475068C>G GRCh38
NC_000010.10:g.75234826C>G , CM000672.1:g.75234826C>G GRCh37
NC_000010.9:g.74904832C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360663.10:c.412-38G>C MANE Select ENSP00000353881.5:n.412-38G>C
ENST00000342558.3:c.412-38G>C ENSP00000343147.3:n.412-38G>C
ENST00000360663.9:c.412-38G>C ENSP00000353881.5:n.412-38G>C
ENST00000394828.6:c.412-38G>C ENSP00000378305.2:n.412-38G>C
ENST00000394829.6:c.412-38G>C ENSP00000378306.2:n.412-38G>C
NM_001142353.2:c.412-38G>C NP_001135825.1:n.412-38G>C
NM_001142354.2:c.412-38G>C NP_001135826.1:n.412-38G>C
NM_001289968.1:c.466-38G>C NP_001276897.1:n.466-38G>C
NM_001289969.1:c.154-38G>C NP_001276898.1:n.154-38G>C
NM_021132.3:c.412-38G>C NP_066955.1:n.412-38G>C
XM_005269944.1:c.412-38G>C XP_005270001.1:n.412-38G>C
XM_011539921.1:c.412-38G>C XP_011538223.1:n.412-38G>C
XM_011539922.1:c.412-38G>C XP_011538224.1:n.412-38G>C
XM_011539923.1:c.412-38G>C XP_011538225.1:n.412-38G>C
XM_017016379.1:c.412-38G>C XP_016871868.1:n.412-38G>C
NM_021132.4:c.412-38G>C MANE Select NP_066955.1:n.412-38G>C
NM_001142353.3:c.412-38G>C NP_001135825.1:n.412-38G>C
NM_001142354.3:c.412-38G>C NP_001135826.1:n.412-38G>C
NM_001289968.2:c.466-38G>C NP_001276897.1:n.466-38G>C
NM_001289969.2:c.154-38G>C NP_001276898.1:n.154-38G>C
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