Canonical Allele Identifier: CA1404303723
Gene: PCCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.136327151C= , CM000665.2:g.136327151C= GRCh38
NC_000003.11:g.136045993C= , CM000665.1:g.136045993C= GRCh37
NC_000003.10:g.137528683C= NCBI36
NG_008939.1:g.81827C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251654.9:c.1199-4C= MANE Select ENSP00000251654.4:n.1199-4C=
ENST00000251654.8:c.1199-4C= ENSP00000251654.4:n.1199-4C=
ENST00000462637.5:c.1130-4C= ENSP00000420391.1:n.1130-4C=
ENST00000466072.5:c.1259-4C= ENSP00000420158.1:n.1259-4C=
ENST00000468777.5:c.1292-4C= ENSP00000419129.1:n.1292-4C=
ENST00000469217.5:c.1259-4C= ENSP00000419027.1:n.1259-4C=
ENST00000471595.5:c.1199-4C= ENSP00000417549.1:n.1199-4C=
ENST00000473073.1:n.1396C=
ENST00000474833.5:n.823+241C=
ENST00000478469.5:c.885-7129C= ENSP00000420759.1:n.885-7129C=
ENST00000482086.5:c.851-4C= ENSP00000417253.1:n.851-4C=
ENST00000483687.5:c.1142-4C= ENSP00000420639.1:n.1142-4C=
ENST00000484181.5:c.1198+241C= ENSP00000417937.1:n.1198+241C=
ENST00000490504.5:c.1028-4C= ENSP00000418307.1:n.1028-4C=
NM_000532.4:c.1199-4C= NP_000523.2:n.1199-4C=
NM_001178014.1:c.1259-4C= NP_001171485.1:n.1259-4C=
NM_000532.5:c.1199-4C= MANE Select NP_000523.2:n.1199-4C=
NM_001178014.2:c.1259-4C= NP_001171485.1:n.1259-4C=