Canonical Allele Identifier: CA435957480

Gene: PCCB

Linked Data

• gnomAD v4: 3-136262029-A-T
• MyVariant Identifiers: chr3:g.135980871A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262029A>T , CM000665.2:g.136262029A>T	GRCh38
NC_000003.11:g.135980871A>T , CM000665.1:g.135980871A>T	GRCh37
NC_000003.10:g.137463561A>T	NCBI36
NG_008939.1:g.16705A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.507A>T MANE Select	ENSP00000251654.4:p.Gly169=
ENST00000251654.8:c.507A>T	ENSP00000251654.4:p.Gly169=
ENST00000459873.1:c.258A>T	ENSP00000419293.1:p.Gly86=
ENST00000462542.5:c.374A>T
ENST00000462637.5:c.438A>T	ENSP00000420391.1:p.Gly146=
ENST00000465176.5:n.469A>T
ENST00000466072.5:c.507A>T	ENSP00000420158.1:p.Gly169=
ENST00000468777.5:c.600A>T	ENSP00000419129.1:p.Gly200=
ENST00000469217.5:c.567A>T	ENSP00000419027.1:p.Gly189=
ENST00000471595.5:c.507A>T	ENSP00000417549.1:p.Gly169=
ENST00000473073.1:n.464A>T
ENST00000474833.5:n.168+11471A>T
ENST00000475214.5:n.421A>T
ENST00000478469.5:c.507A>T	ENSP00000420759.1:p.Gly169=
ENST00000482086.5:c.159A>T	ENSP00000417253.1:p.Gly53=
ENST00000483687.5:c.450A>T	ENSP00000420639.1:p.Gly150=
ENST00000484181.5:c.507A>T	ENSP00000417937.1:p.Gly169=
ENST00000490504.5:c.372+5406A>T	ENSP00000418307.1:n.372+5406A>T
NM_000532.4:c.507A>T	NP_000523.2:p.Gly169=
NM_001178014.1:c.567A>T	NP_001171485.1:p.Gly189=
XM_011512873.1:c.507A>T	XP_011511175.1:p.Gly169=
XM_011512873.2:c.507A>T	XP_011511175.1:p.Gly169=
NM_000532.5:c.507A>T MANE Select	NP_000523.2:p.Gly169=
NM_001178014.2:c.567A>T	NP_001171485.1:p.Gly189=