Canonical Allele Identifier: CA6943129
Gene: PDS5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32709999A>G , CM000675.2:g.32709999A>G GRCh38
NC_000013.10:g.33284136A>G , CM000675.1:g.33284136A>G GRCh37
NC_000013.9:g.32182136A>G NCBI36
NG_021308.1:g.128573A>G
NG_021308.2:g.128573A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315596.15:c.2016A>G MANE Select ENSP00000313851.10:p.Ser672=
ENST00000315596.14:c.2016A>G ENSP00000313851.10:p.Ser672=
ENST00000450460.5:c.2016A>G ENSP00000401619.1:p.Ser672=
ENST00000481616.1:n.615A>G
NM_015032.3:c.2016A>G NP_055847.1:p.Ser672=
XM_005266298.3:c.2016A>G XP_005266355.1:p.Ser672=
XM_011534999.1:c.2016A>G XP_011533301.1:p.Ser672=
XM_011535000.1:c.2016A>G XP_011533302.1:p.Ser672=
XM_011535001.1:c.2016A>G XP_011533303.1:p.Ser672=
XM_011535002.1:c.1188A>G XP_011533304.1:p.Ser396=
XM_005266298.4:c.2016A>G XP_005266355.1:p.Ser672=
XM_011534999.2:c.2016A>G XP_011533301.1:p.Ser672=
XM_011535000.2:c.2016A>G XP_011533302.1:p.Ser672=
XM_011535002.3:c.1188A>G XP_011533304.1:p.Ser396=
XM_017020448.1:c.2016A>G XP_016875937.1:p.Ser672=
XM_017020449.1:c.2016A>G XP_016875938.1:p.Ser672=
XM_017020450.1:c.2016A>G XP_016875939.1:p.Ser672=
XM_017020451.1:c.2016A>G XP_016875940.1:p.Ser672=
XM_017020452.2:c.2016A>G XP_016875941.1:p.Ser672=
XM_017020453.1:c.2016A>G XP_016875942.1:p.Ser672=
NM_015032.4:c.2016A>G MANE Select NP_055847.1:p.Ser672=