Canonical Allele Identifier: CA354739619

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980834G>C (hg19) ; chr3:g.136261992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261992G>C , CM000665.2:g.136261992G>C	GRCh38
NC_000003.11:g.135980834G>C , CM000665.1:g.135980834G>C	GRCh37
NC_000003.10:g.137463524G>C	NCBI36
NG_008939.1:g.16668G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.470G>C MANE Select	ENSP00000251654.4:p.Gly157Ala
ENST00000251654.8:c.470G>C	ENSP00000251654.4:p.Gly157Ala
ENST00000459873.1:c.221G>C	ENSP00000419293.1:p.Gly74Ala
ENST00000462542.5:c.337G>C
ENST00000462637.5:c.401G>C	ENSP00000420391.1:p.Gly134Ala
ENST00000465176.5:n.432G>C
ENST00000465423.5:c.557G>C	ENSP00000419263.1:p.Gly186Ala
ENST00000466072.5:c.470G>C	ENSP00000420158.1:p.Gly157Ala
ENST00000468777.5:c.563G>C	ENSP00000419129.1:p.Gly188Ala
ENST00000469217.5:c.530G>C	ENSP00000419027.1:p.Gly177Ala
ENST00000471595.5:c.470G>C	ENSP00000417549.1:p.Gly157Ala
ENST00000473073.1:n.427G>C
ENST00000474833.5:n.168+11434G>C
ENST00000475214.5:n.384G>C
ENST00000478469.5:c.470G>C	ENSP00000420759.1:p.Gly157Ala
ENST00000482086.5:c.122G>C	ENSP00000417253.1:p.Gly41Ala
ENST00000483687.5:c.413G>C	ENSP00000420639.1:p.Gly138Ala
ENST00000484181.5:c.470G>C	ENSP00000417937.1:p.Gly157Ala
ENST00000490504.5:c.372+5369G>C	ENSP00000418307.1:n.372+5369G>C
ENST00000494742.5:c.221G>C	ENSP00000418020.1:p.Gly74Ala
NM_000532.4:c.470G>C	NP_000523.2:p.Gly157Ala
NM_001178014.1:c.530G>C	NP_001171485.1:p.Gly177Ala
XM_011512873.1:c.470G>C	XP_011511175.1:p.Gly157Ala
XM_011512873.2:c.470G>C	XP_011511175.1:p.Gly157Ala
NM_000532.5:c.470G>C MANE Select	NP_000523.2:p.Gly157Ala
NM_001178014.2:c.530G>C	NP_001171485.1:p.Gly177Ala