Canonical Allele Identifier: CA435957475

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980862C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262020C>T , CM000665.2:g.136262020C>T	GRCh38
NC_000003.11:g.135980862C>T , CM000665.1:g.135980862C>T	GRCh37
NC_000003.10:g.137463552C>T	NCBI36
NG_008939.1:g.16696C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.498C>T MANE Select	ENSP00000251654.4:p.Ile166=
ENST00000251654.8:c.498C>T	ENSP00000251654.4:p.Ile166=
ENST00000459873.1:c.249C>T	ENSP00000419293.1:p.Ile83=
ENST00000462542.5:c.365C>T
ENST00000462637.5:c.429C>T	ENSP00000420391.1:p.Ile143=
ENST00000465176.5:n.460C>T
ENST00000466072.5:c.498C>T	ENSP00000420158.1:p.Ile166=
ENST00000468777.5:c.591C>T	ENSP00000419129.1:p.Ile197=
ENST00000469217.5:c.558C>T	ENSP00000419027.1:p.Ile186=
ENST00000471595.5:c.498C>T	ENSP00000417549.1:p.Ile166=
ENST00000473073.1:n.455C>T
ENST00000474833.5:n.168+11462C>T
ENST00000475214.5:n.412C>T
ENST00000478469.5:c.498C>T	ENSP00000420759.1:p.Ile166=
ENST00000482086.5:c.150C>T	ENSP00000417253.1:p.Ile50=
ENST00000483687.5:c.441C>T	ENSP00000420639.1:p.Ile147=
ENST00000484181.5:c.498C>T	ENSP00000417937.1:p.Ile166=
ENST00000490504.5:c.372+5397C>T	ENSP00000418307.1:n.372+5397C>T
ENST00000494742.5:c.249C>T	ENSP00000418020.1:p.Ile83=
NM_000532.4:c.498C>T	NP_000523.2:p.Ile166=
NM_001178014.1:c.558C>T	NP_001171485.1:p.Ile186=
XM_011512873.1:c.498C>T	XP_011511175.1:p.Ile166=
XM_011512873.2:c.498C>T	XP_011511175.1:p.Ile166=
NM_000532.5:c.498C>T MANE Select	NP_000523.2:p.Ile166=
NM_001178014.2:c.558C>T	NP_001171485.1:p.Ile186=