Canonical Allele Identifier: CA2053548553
Gene: POC1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.89503524G= , CM000674.2:g.89503524G= GRCh38
NC_000012.11:g.89897301G= , CM000674.1:g.89897301G= GRCh37
NC_000012.10:g.88421432G= NCBI36
NG_041783.1:g.27739C=

Transcript Alleles

HGVS Amino-acid change
ENST00000313546.8:c.101-6182C= MANE Select ENSP00000323302.3:n.101-6182C=
ENST00000313546.7:c.101-6182C= ENSP00000323302.3:n.101-6182C=
ENST00000393179.8:c.-118-11409C= ENSP00000376877.4:n.-118-11409C=
ENST00000539190.6:n.199-6182C=
ENST00000546830.1:c.101-6182C= ENSP00000449256.1:n.101-6182C=
ENST00000547274.5:c.101-11409C= ENSP00000449648.1:n.101-11409C=
ENST00000547496.5:c.101-11409C= ENSP00000447437.1:n.101-11409C=
ENST00000548715.5:c.101-11409C= ENSP00000449945.1:n.101-11409C=
ENST00000549035.1:c.-26-6182C= ENSP00000447916.1:n.-26-6182C=
ENST00000549504.1:c.-118-11409C= ENSP00000450118.1:n.-118-11409C=
ENST00000552563.1:n.297-11409C=
NM_001199777.1:c.-26-6182C= NP_001186706.1:n.-26-6182C=
NM_172240.2:c.101-6182C= NP_758440.1:n.101-6182C=
NR_037659.1:n.468-11409C=
NR_037660.1:n.449-11409C=
NM_172240.3:c.101-6182C= MANE Select NP_758440.1:n.101-6182C=
NM_001199777.2:c.-26-6182C= NP_001186706.1:n.-26-6182C=
NR_037659.2:n.253-11409C=
NR_037660.2:n.312-11409C=