Canonical Allele Identifier: CA435957459

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980850G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262008G>C , CM000665.2:g.136262008G>C	GRCh38
NC_000003.11:g.135980850G>C , CM000665.1:g.135980850G>C	GRCh37
NC_000003.10:g.137463540G>C	NCBI36
NG_008939.1:g.16684G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.486G>C MANE Select	ENSP00000251654.4:p.Gly162=
ENST00000251654.8:c.486G>C	ENSP00000251654.4:p.Gly162=
ENST00000459873.1:c.237G>C	ENSP00000419293.1:p.Gly79=
ENST00000462542.5:c.353G>C
ENST00000462637.5:c.417G>C	ENSP00000420391.1:p.Gly139=
ENST00000465176.5:n.448G>C
ENST00000465423.5:c.573G>C	ENSP00000419263.1:p.Gly191=
ENST00000466072.5:c.486G>C	ENSP00000420158.1:p.Gly162=
ENST00000468777.5:c.579G>C	ENSP00000419129.1:p.Gly193=
ENST00000469217.5:c.546G>C	ENSP00000419027.1:p.Gly182=
ENST00000471595.5:c.486G>C	ENSP00000417549.1:p.Gly162=
ENST00000473073.1:n.443G>C
ENST00000474833.5:n.168+11450G>C
ENST00000475214.5:n.400G>C
ENST00000478469.5:c.486G>C	ENSP00000420759.1:p.Gly162=
ENST00000482086.5:c.138G>C	ENSP00000417253.1:p.Gly46=
ENST00000483687.5:c.429G>C	ENSP00000420639.1:p.Gly143=
ENST00000484181.5:c.486G>C	ENSP00000417937.1:p.Gly162=
ENST00000490504.5:c.372+5385G>C	ENSP00000418307.1:n.372+5385G>C
ENST00000494742.5:c.237G>C	ENSP00000418020.1:p.Gly79=
NM_000532.4:c.486G>C	NP_000523.2:p.Gly162=
NM_001178014.1:c.546G>C	NP_001171485.1:p.Gly182=
XM_011512873.1:c.486G>C	XP_011511175.1:p.Gly162=
XM_011512873.2:c.486G>C	XP_011511175.1:p.Gly162=
NM_000532.5:c.486G>C MANE Select	NP_000523.2:p.Gly162=
NM_001178014.2:c.546G>C	NP_001171485.1:p.Gly182=