Canonical Allele Identifier: CA950300892
Gene: POC1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89503544_89503583del , CM000674.2:g.89503544_89503583del GRCh38
NC_000012.11:g.89897321_89897360del , CM000674.1:g.89897321_89897360del GRCh37
NC_000012.10:g.88421452_88421491del NCBI36
NG_041783.1:g.27687_27726del

Transcript Alleles

HGVS Amino-acid change
ENST00000313546.8:c.101-6234_101-6195del MANE Select ENSP00000323302.3:n.101-6234_101-6195del
ENST00000313546.7:c.101-6234_101-6195del ENSP00000323302.3:n.101-6234_101-6195del
ENST00000393179.8:c.-118-11461_-118-11422del ENSP00000376877.4:n.-118-11461_-118-11422del
ENST00000539190.6:n.199-6234_199-6195del
ENST00000546830.1:c.101-6234_101-6195del ENSP00000449256.1:n.101-6234_101-6195del
ENST00000547274.5:c.101-11461_101-11422del ENSP00000449648.1:n.101-11461_101-11422del
ENST00000547496.5:c.101-11461_101-11422del ENSP00000447437.1:n.101-11461_101-11422del
ENST00000548715.5:c.101-11461_101-11422del ENSP00000449945.1:n.101-11461_101-11422del
ENST00000549035.1:c.-26-6234_-26-6195del ENSP00000447916.1:n.-26-6234_-26-6195del
ENST00000549504.1:c.-118-11461_-118-11422del ENSP00000450118.1:n.-118-11461_-118-11422del
ENST00000552563.1:n.297-11461_297-11422del
NM_001199777.1:c.-26-6234_-26-6195del NP_001186706.1:n.-26-6234_-26-6195del
NM_172240.2:c.101-6234_101-6195del NP_758440.1:n.101-6234_101-6195del
NR_037659.1:n.468-11461_468-11422del
NR_037660.1:n.449-11461_449-11422del
NM_172240.3:c.101-6234_101-6195del MANE Select NP_758440.1:n.101-6234_101-6195del
NM_001199777.2:c.-26-6234_-26-6195del NP_001186706.1:n.-26-6234_-26-6195del
NR_037659.2:n.253-11461_253-11422del
NR_037660.2:n.312-11461_312-11422del