Canonical Allele Identifier: CA435841731

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.136047626G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136328784G>C , CM000665.2:g.136328784G>C	GRCh38
NC_000003.11:g.136047626G>C , CM000665.1:g.136047626G>C	GRCh37
NC_000003.10:g.137530316G>C	NCBI36
NG_008939.1:g.83460G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1425G>C MANE Select	ENSP00000251654.4:p.Gly475=
ENST00000251654.8:c.1425G>C	ENSP00000251654.4:p.Gly475=
ENST00000462637.5:c.1356G>C	ENSP00000420391.1:p.Gly452=
ENST00000466072.5:c.1485G>C	ENSP00000420158.1:p.Gly495=
ENST00000468777.5:c.1518G>C	ENSP00000419129.1:p.Gly506=
ENST00000469217.5:c.1485G>C	ENSP00000419027.1:p.Gly495=
ENST00000471595.5:c.1425G>C	ENSP00000417549.1:p.Gly475=
ENST00000473073.1:n.1626G>C
ENST00000478469.5:c.885-5496G>C	ENSP00000420759.1:n.885-5496G>C
ENST00000482086.5:c.1077G>C	ENSP00000417253.1:p.Gly359=
ENST00000483687.5:c.1368G>C	ENSP00000420639.1:p.Gly456=
ENST00000484181.5:c.*106G>C	ENSP00000417937.1:n.*106G>C
ENST00000490504.5:c.1254G>C	ENSP00000418307.1:p.Gly418=
NM_000532.4:c.1425G>C	NP_000523.2:p.Gly475=
NM_001178014.1:c.1485G>C	NP_001171485.1:p.Gly495=
NM_000532.5:c.1425G>C MANE Select	NP_000523.2:p.Gly475=
NM_001178014.2:c.1485G>C	NP_001171485.1:p.Gly495=