Canonical Allele Identifier: CA84266984

Gene: PCCB

Linked Data

• dbSNP Id: rs904295924
• gnomAD v2: 3-135980741-G-A
• gnomAD v3: 3-136261899-G-A
• gnomAD v4: 3-136261899-G-A
• MyVariant Identifiers: chr3:g.135980741G>A (hg19) ; chr3:g.136261899G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261899G>A , CM000665.2:g.136261899G>A	GRCh38
NC_000003.11:g.135980741G>A , CM000665.1:g.135980741G>A	GRCh37
NC_000003.10:g.137463431G>A	NCBI36
NG_008939.1:g.16575G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.430-53G>A MANE Select	ENSP00000251654.4:n.430-53G>A
ENST00000251654.8:c.430-53G>A	ENSP00000251654.4:n.430-53G>A
ENST00000459873.1:c.181-53G>A	ENSP00000419293.1:n.181-53G>A
ENST00000462542.5:c.297-53G>A
ENST00000462637.5:c.361-53G>A	ENSP00000420391.1:n.361-53G>A
ENST00000465176.5:n.392-53G>A
ENST00000465423.5:c.517-53G>A	ENSP00000419263.1:n.517-53G>A
ENST00000466072.5:c.430-53G>A	ENSP00000420158.1:n.430-53G>A
ENST00000468777.5:c.523-53G>A	ENSP00000419129.1:n.523-53G>A
ENST00000469217.5:c.490-53G>A	ENSP00000419027.1:n.490-53G>A
ENST00000471595.5:c.430-53G>A	ENSP00000417549.1:n.430-53G>A
ENST00000473073.1:n.387-53G>A
ENST00000474833.5:n.168+11341G>A
ENST00000475214.5:n.344-53G>A
ENST00000478469.5:c.430-53G>A	ENSP00000420759.1:n.430-53G>A
ENST00000482086.5:c.94-65G>A	ENSP00000417253.1:n.94-65G>A
ENST00000483687.5:c.373-53G>A	ENSP00000420639.1:n.373-53G>A
ENST00000484181.5:c.430-53G>A	ENSP00000417937.1:n.430-53G>A
ENST00000490504.5:c.372+5276G>A	ENSP00000418307.1:n.372+5276G>A
ENST00000494742.5:c.181-53G>A	ENSP00000418020.1:n.181-53G>A
NM_000532.4:c.430-53G>A	NP_000523.2:n.430-53G>A
NM_001178014.1:c.490-53G>A	NP_001171485.1:n.490-53G>A
XM_011512873.1:c.430-53G>A	XP_011511175.1:n.430-53G>A
XM_011512873.2:c.430-53G>A	XP_011511175.1:n.430-53G>A
NM_000532.5:c.430-53G>A MANE Select	NP_000523.2:n.430-53G>A
NM_001178014.2:c.490-53G>A	NP_001171485.1:n.490-53G>A