Canonical Allele Identifier: CA2053548659

Gene: POC1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.89503580G= , CM000674.2:g.89503580G=	GRCh38
NC_000012.11:g.89897357G= , CM000674.1:g.89897357G=	GRCh37
NC_000012.10:g.88421488G=	NCBI36
NG_041783.1:g.27683C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313546.8:c.101-6238C= MANE Select	ENSP00000323302.3:n.101-6238C=
ENST00000313546.7:c.101-6238C=	ENSP00000323302.3:n.101-6238C=
ENST00000393179.8:c.-118-11465C=	ENSP00000376877.4:n.-118-11465C=
ENST00000539190.6:n.199-6238C=
ENST00000546830.1:c.101-6238C=	ENSP00000449256.1:n.101-6238C=
ENST00000547274.5:c.101-11465C=	ENSP00000449648.1:n.101-11465C=
ENST00000547496.5:c.101-11465C=	ENSP00000447437.1:n.101-11465C=
ENST00000548715.5:c.101-11465C=	ENSP00000449945.1:n.101-11465C=
ENST00000549035.1:c.-26-6238C=	ENSP00000447916.1:n.-26-6238C=
ENST00000549504.1:c.-118-11465C=	ENSP00000450118.1:n.-118-11465C=
ENST00000552563.1:n.297-11465C=
NM_001199777.1:c.-26-6238C=	NP_001186706.1:n.-26-6238C=
NM_172240.2:c.101-6238C=	NP_758440.1:n.101-6238C=
NR_037659.1:n.468-11465C=
NR_037660.1:n.449-11465C=
NM_172240.3:c.101-6238C= MANE Select	NP_758440.1:n.101-6238C=
NM_001199777.2:c.-26-6238C=	NP_001186706.1:n.-26-6238C=
NR_037659.2:n.253-11465C=
NR_037660.2:n.312-11465C=