Canonical Allele Identifier: CA354739583

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980819G>C (hg19) ; chr3:g.136261977G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261977G>C , CM000665.2:g.136261977G>C	GRCh38
NC_000003.11:g.135980819G>C , CM000665.1:g.135980819G>C	GRCh37
NC_000003.10:g.137463509G>C	NCBI36
NG_008939.1:g.16653G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.455G>C MANE Select	ENSP00000251654.4:p.Gly152Ala
ENST00000251654.8:c.455G>C	ENSP00000251654.4:p.Gly152Ala
ENST00000459873.1:c.206G>C	ENSP00000419293.1:p.Gly69Ala
ENST00000462542.5:c.322G>C
ENST00000462637.5:c.386G>C	ENSP00000420391.1:p.Gly129Ala
ENST00000465176.5:n.417G>C
ENST00000465423.5:c.542G>C	ENSP00000419263.1:p.Gly181Ala
ENST00000466072.5:c.455G>C	ENSP00000420158.1:p.Gly152Ala
ENST00000468777.5:c.548G>C	ENSP00000419129.1:p.Gly183Ala
ENST00000469217.5:c.515G>C	ENSP00000419027.1:p.Gly172Ala
ENST00000471595.5:c.455G>C	ENSP00000417549.1:p.Gly152Ala
ENST00000473073.1:n.412G>C
ENST00000474833.5:n.168+11419G>C
ENST00000475214.5:n.369G>C
ENST00000478469.5:c.455G>C	ENSP00000420759.1:p.Gly152Ala
ENST00000482086.5:c.107G>C	ENSP00000417253.1:p.Gly36Ala
ENST00000483687.5:c.398G>C	ENSP00000420639.1:p.Gly133Ala
ENST00000484181.5:c.455G>C	ENSP00000417937.1:p.Gly152Ala
ENST00000490504.5:c.372+5354G>C	ENSP00000418307.1:n.372+5354G>C
ENST00000494742.5:c.206G>C	ENSP00000418020.1:p.Gly69Ala
NM_000532.4:c.455G>C	NP_000523.2:p.Gly152Ala
NM_001178014.1:c.515G>C	NP_001171485.1:p.Gly172Ala
XM_011512873.1:c.455G>C	XP_011511175.1:p.Gly152Ala
XM_011512873.2:c.455G>C	XP_011511175.1:p.Gly152Ala
NM_000532.5:c.455G>C MANE Select	NP_000523.2:p.Gly152Ala
NM_001178014.2:c.515G>C	NP_001171485.1:p.Gly172Ala