Canonical Allele Identifier: CA354739875

Gene: PCCB

Linked Data

• ClinVar Variation Id: 2677524
• ClinVar RCV Id: RCV003471659
• gnomAD v4: 3-136262021-C-T
• MyVariant Identifiers: chr3:g.135980863C>T (hg19) ; chr3:g.136262021C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262021C>T , CM000665.2:g.136262021C>T	GRCh38
NC_000003.11:g.135980863C>T , CM000665.1:g.135980863C>T	GRCh37
NC_000003.10:g.137463553C>T	NCBI36
NG_008939.1:g.16697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.499C>T MANE Select	ENSP00000251654.4:p.Gln167Ter
ENST00000251654.8:c.499C>T	ENSP00000251654.4:p.Gln167Ter
ENST00000459873.1:c.250C>T	ENSP00000419293.1:p.Gln84Ter
ENST00000462542.5:c.366C>T
ENST00000462637.5:c.430C>T	ENSP00000420391.1:p.Gln144Ter
ENST00000465176.5:n.461C>T
ENST00000466072.5:c.499C>T	ENSP00000420158.1:p.Gln167Ter
ENST00000468777.5:c.592C>T	ENSP00000419129.1:p.Gln198Ter
ENST00000469217.5:c.559C>T	ENSP00000419027.1:p.Gln187Ter
ENST00000471595.5:c.499C>T	ENSP00000417549.1:p.Gln167Ter
ENST00000473073.1:n.456C>T
ENST00000474833.5:n.168+11463C>T
ENST00000475214.5:n.413C>T
ENST00000478469.5:c.499C>T	ENSP00000420759.1:p.Gln167Ter
ENST00000482086.5:c.151C>T	ENSP00000417253.1:p.Gln51Ter
ENST00000483687.5:c.442C>T	ENSP00000420639.1:p.Gln148Ter
ENST00000484181.5:c.499C>T	ENSP00000417937.1:p.Gln167Ter
ENST00000490504.5:c.372+5398C>T	ENSP00000418307.1:n.372+5398C>T
ENST00000494742.5:c.250C>T	ENSP00000418020.1:p.Gln84Ter
NM_000532.4:c.499C>T	NP_000523.2:p.Gln167Ter
NM_001178014.1:c.559C>T	NP_001171485.1:p.Gln187Ter
XM_011512873.1:c.499C>T	XP_011511175.1:p.Gln167Ter
XM_011512873.2:c.499C>T	XP_011511175.1:p.Gln167Ter
NM_000532.5:c.499C>T MANE Select	NP_000523.2:p.Gln167Ter
NM_001178014.2:c.559C>T	NP_001171485.1:p.Gln187Ter