Canonical Allele Identifier: CA2494166152

Gene: PPM1B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44225251C>A , CM000664.2:g.44225251C>A	GRCh38
NC_000002.11:g.44452390C>A , CM000664.1:g.44452390C>A	GRCh37
NC_000002.10:g.44305894C>A	NCBI36
NG_011678.1:g.61391C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282412.9:c.1135-5162C>A MANE Select	ENSP00000282412.4:n.1135-5162C>A
ENST00000649044.1:c.1134+6714C>A	ENSP00000497083.1:n.1134+6714C>A
ENST00000282412.8:c.1135-5162C>A	ENSP00000282412.4:n.1135-5162C>A
ENST00000345249.8:c.274-5162C>A	ENSP00000326089.4:n.274-5162C>A
ENST00000378540.8:n.1546+6714C>A
ENST00000378551.6:c.1134+6714C>A	ENSP00000367813.2:n.1134+6714C>A
ENST00000409432.7:c.1135-4742C>A	ENSP00000387287.3:n.1135-4742C>A
ENST00000459690.5:n.270+6714C>A
ENST00000487286.1:n.379+6714C>A
NM_001033557.2:c.1135-4742C>A	NP_001028729.1:n.1135-4742C>A
NM_002706.5:c.1135-5162C>A	NP_002697.1:n.1135-5162C>A
NM_177968.3:c.1134+6714C>A	NP_808907.1:n.1134+6714C>A
NM_177969.3:c.274-5162C>A	NP_808908.1:n.274-5162C>A
XM_011532936.1:c.1134+6714C>A	XP_011531238.1:n.1134+6714C>A
XM_011532936.3:c.1134+6714C>A	XP_011531238.1:n.1134+6714C>A
XM_017004395.2:c.1159-5162C>A	XP_016859884.1:n.1159-5162C>A
XM_017004396.2:c.1158+6714C>A	XP_016859885.1:n.1158+6714C>A
XM_017004397.2:c.1158+6714C>A	XP_016859886.1:n.1158+6714C>A
NM_002706.6:c.1135-5162C>A MANE Select	NP_002697.1:n.1135-5162C>A
NM_001033557.3:c.1135-4742C>A	NP_001028729.1:n.1135-4742C>A
NM_177968.4:c.1134+6714C>A	NP_808907.1:n.1134+6714C>A
NM_177969.4:c.274-5162C>A	NP_808908.1:n.274-5162C>A