Canonical Allele Identifier: CA354739666

Gene: PCCB

Linked Data

• gnomAD v4: 3-136262009-G-T
• MyVariant Identifiers: chr3:g.135980851G>T (hg19) ; chr3:g.136262009G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262009G>T , CM000665.2:g.136262009G>T	GRCh38
NC_000003.11:g.135980851G>T , CM000665.1:g.135980851G>T	GRCh37
NC_000003.10:g.137463541G>T	NCBI36
NG_008939.1:g.16685G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.487G>T MANE Select	ENSP00000251654.4:p.Gly163Ter
ENST00000251654.8:c.487G>T	ENSP00000251654.4:p.Gly163Ter
ENST00000459873.1:c.238G>T	ENSP00000419293.1:p.Gly80Ter
ENST00000462542.5:c.354G>T
ENST00000462637.5:c.418G>T	ENSP00000420391.1:p.Gly140Ter
ENST00000465176.5:n.449G>T
ENST00000465423.5:c.574G>T
ENST00000466072.5:c.487G>T	ENSP00000420158.1:p.Gly163Ter
ENST00000468777.5:c.580G>T	ENSP00000419129.1:p.Gly194Ter
ENST00000469217.5:c.547G>T	ENSP00000419027.1:p.Gly183Ter
ENST00000471595.5:c.487G>T	ENSP00000417549.1:p.Gly163Ter
ENST00000473073.1:n.444G>T
ENST00000474833.5:n.168+11451G>T
ENST00000475214.5:n.401G>T
ENST00000478469.5:c.487G>T	ENSP00000420759.1:p.Gly163Ter
ENST00000482086.5:c.139G>T	ENSP00000417253.1:p.Gly47Ter
ENST00000483687.5:c.430G>T	ENSP00000420639.1:p.Gly144Ter
ENST00000484181.5:c.487G>T	ENSP00000417937.1:p.Gly163Ter
ENST00000490504.5:c.372+5386G>T	ENSP00000418307.1:n.372+5386G>T
ENST00000494742.5:c.238G>T	ENSP00000418020.1:p.Gly80Ter
NM_000532.4:c.487G>T	NP_000523.2:p.Gly163Ter
NM_001178014.1:c.547G>T	NP_001171485.1:p.Gly183Ter
XM_011512873.1:c.487G>T	XP_011511175.1:p.Gly163Ter
XM_011512873.2:c.487G>T	XP_011511175.1:p.Gly163Ter
NM_000532.5:c.487G>T MANE Select	NP_000523.2:p.Gly163Ter
NM_001178014.2:c.547G>T	NP_001171485.1:p.Gly183Ter