Canonical Allele Identifier: CA693226328

Gene: POC1B

Linked Data

• dbSNP Id: rs1301976764
• MyVariant Identifiers: chr12:g.89897290C>T (hg19) ; chr12:g.89503513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.89503513C>T , CM000674.2:g.89503513C>T	GRCh38
NC_000012.11:g.89897290C>T , CM000674.1:g.89897290C>T	GRCh37
NC_000012.10:g.88421421C>T	NCBI36
NG_041783.1:g.27750G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313546.8:c.101-6171G>A MANE Select	ENSP00000323302.3:n.101-6171G>A
ENST00000313546.7:c.101-6171G>A	ENSP00000323302.3:n.101-6171G>A
ENST00000393179.8:c.-118-11398G>A	ENSP00000376877.4:n.-118-11398G>A
ENST00000539190.6:n.199-6171G>A
ENST00000546830.1:c.101-6171G>A	ENSP00000449256.1:n.101-6171G>A
ENST00000547274.5:c.101-11398G>A	ENSP00000449648.1:n.101-11398G>A
ENST00000547496.5:c.101-11398G>A	ENSP00000447437.1:n.101-11398G>A
ENST00000548715.5:c.101-11398G>A	ENSP00000449945.1:n.101-11398G>A
ENST00000549035.1:c.-26-6171G>A	ENSP00000447916.1:n.-26-6171G>A
ENST00000549504.1:c.-118-11398G>A	ENSP00000450118.1:n.-118-11398G>A
ENST00000552563.1:n.297-11398G>A
NM_001199777.1:c.-26-6171G>A	NP_001186706.1:n.-26-6171G>A
NM_172240.2:c.101-6171G>A	NP_758440.1:n.101-6171G>A
NR_037659.1:n.468-11398G>A
NR_037660.1:n.449-11398G>A
NM_172240.3:c.101-6171G>A MANE Select	NP_758440.1:n.101-6171G>A
NM_001199777.2:c.-26-6171G>A	NP_001186706.1:n.-26-6171G>A
NR_037659.2:n.253-11398G>A
NR_037660.2:n.312-11398G>A